STRINGSTRING
Q5KPQ9_CRYNJ Q5KPQ9_CRYNJ Q5KPR9_CRYNJ Q5KPR9_CRYNJ Q5KPS5_CRYNJ Q5KPS5_CRYNJ A0A0S2LHW3 A0A0S2LHW3 A0A0S2LI43 A0A0S2LI43 A0A0S2LII0 A0A0S2LII0 A0A0S2LIJ5 A0A0S2LIJ5 A0A0S2LIL8 A0A0S2LIL8 A0A0S2LIR2 A0A0S2LIR2 A0A0S2LIT1 A0A0S2LIT1 A0A0S2LIX3 A0A0S2LIX3 A0A0S2LIY7 A0A0S2LIY7 A0A0S2M5A9 A0A0S2M5A9 A0A0S2M5L1 A0A0S2M5L1 A0A0S2M5R0 A0A0S2M5R0 A0A0S2M5Z0 A0A0S2M5Z0 A0A0S2M611 A0A0S2M611 A0A0S2M691 A0A0S2M691 ALG14 ALG14 CYN1 CYN1 TIM50 TIM50 GPA1 GPA1 MDM10 MDM10 MDM12 MDM12 MDM34 MDM34 MMM1 MMM1 NPL4 NPL4 PAM17 PAM17 SAR1 SAR1 SEC23 SEC23 SEC24 SEC24 SNF7 SNF7 SNX3 SNX3 TIM22 TIM22 TIM54 TIM54 TIM9 TIM9 TIM10 TIM10 SEC13 SEC13 Q5K6T7_CRYNJ Q5K6T7_CRYNJ Q5K6T9_CRYNJ Q5K6T9_CRYNJ Q5K6Y2_CRYNJ Q5K6Y2_CRYNJ Q5K6Z4_CRYNJ Q5K6Z4_CRYNJ Q5K701_CRYNJ Q5K701_CRYNJ Q5K720_CRYNJ Q5K720_CRYNJ Q5K728_CRYNJ Q5K728_CRYNJ Q5K757_CRYNJ Q5K757_CRYNJ Q5K779_CRYNJ Q5K779_CRYNJ Q5K7H4_CRYNJ Q5K7H4_CRYNJ Q5K7H5_CRYNJ Q5K7H5_CRYNJ Q5K7J0_CRYNJ Q5K7J0_CRYNJ Q5K7M2_CRYNJ Q5K7M2_CRYNJ Q5K7N6_CRYNJ Q5K7N6_CRYNJ Q5K7Q5_CRYNJ Q5K7Q5_CRYNJ Q5K7S8_CRYNJ Q5K7S8_CRYNJ Q5K7X0_CRYNJ Q5K7X0_CRYNJ Q5K7Z1_CRYNJ Q5K7Z1_CRYNJ Q5K822_CRYNJ Q5K822_CRYNJ Q5K888_CRYNJ Q5K888_CRYNJ Q5K889_CRYNJ Q5K889_CRYNJ Q5K8G6_CRYNJ Q5K8G6_CRYNJ Q5K8H0_CRYNJ Q5K8H0_CRYNJ Q5K8J0_CRYNJ Q5K8J0_CRYNJ Q5K8K8_CRYNJ Q5K8K8_CRYNJ Q5K8L7_CRYNJ Q5K8L7_CRYNJ Q5K8Q1_CRYNJ Q5K8Q1_CRYNJ VMA9 VMA9 Q5K8T1_CRYNJ Q5K8T1_CRYNJ Q5K8U4_CRYNJ Q5K8U4_CRYNJ Q5K8W3_CRYNJ Q5K8W3_CRYNJ Q5K8Y5_CRYNJ Q5K8Y5_CRYNJ Q5K906_CRYNJ Q5K906_CRYNJ Q5K938_CRYNJ Q5K938_CRYNJ Q5K946_CRYNJ Q5K946_CRYNJ Q5K9E5_CRYNJ Q5K9E5_CRYNJ Q5K9H6_CRYNJ Q5K9H6_CRYNJ Q5K9K1_CRYNJ Q5K9K1_CRYNJ Q5K9K5_CRYNJ Q5K9K5_CRYNJ Q5K9Y4_CRYNJ Q5K9Y4_CRYNJ Q5KA21_CRYNJ Q5KA21_CRYNJ Q5KA29_CRYNJ Q5KA29_CRYNJ Q5KA71_CRYNJ Q5KA71_CRYNJ Q5KA77_CRYNJ Q5KA77_CRYNJ Q5KAA7_CRYNJ Q5KAA7_CRYNJ Q5KAB5_CRYNJ Q5KAB5_CRYNJ Q5KAG9_CRYNJ Q5KAG9_CRYNJ Q5KAJ6_CRYNJ Q5KAJ6_CRYNJ Q5KAU1_CRYNJ Q5KAU1_CRYNJ Q5KAX9_CRYNJ Q5KAX9_CRYNJ Q5KB19_CRYNJ Q5KB19_CRYNJ Q5KB78_CRYNJ Q5KB78_CRYNJ Q5KBA0_CRYNJ Q5KBA0_CRYNJ Q5KBG5_CRYNJ Q5KBG5_CRYNJ Q5KBG8_CRYNJ Q5KBG8_CRYNJ Q5KBH1_CRYNJ Q5KBH1_CRYNJ Q5KBI9_CRYNJ Q5KBI9_CRYNJ Q5KBP6_CRYNJ Q5KBP6_CRYNJ Q5KBP7_CRYNJ Q5KBP7_CRYNJ Q5KBR2_CRYNJ Q5KBR2_CRYNJ Q5KBR3_CRYNJ Q5KBR3_CRYNJ Q5KBW0_CRYNJ Q5KBW0_CRYNJ Q5KC20_CRYNJ Q5KC20_CRYNJ Q5KC44_CRYNJ Q5KC44_CRYNJ Q5KC66_CRYNJ Q5KC66_CRYNJ Q5KC69_CRYNJ Q5KC69_CRYNJ Q5KCD5_CRYNJ Q5KCD5_CRYNJ Q5KCF2_CRYNJ Q5KCF2_CRYNJ Q5KCH4_CRYNJ Q5KCH4_CRYNJ Q5KCK0_CRYNJ Q5KCK0_CRYNJ Q5KCK9_CRYNJ Q5KCK9_CRYNJ Q5KCR0_CRYNJ Q5KCR0_CRYNJ Q5KCT8_CRYNJ Q5KCT8_CRYNJ Q5KCX6_CRYNJ Q5KCX6_CRYNJ Q5KCZ2_CRYNJ Q5KCZ2_CRYNJ Q5KCZ3_CRYNJ Q5KCZ3_CRYNJ Q5KD38_CRYNJ Q5KD38_CRYNJ Q5KD54_CRYNJ Q5KD54_CRYNJ Q5KD71_CRYNJ Q5KD71_CRYNJ Q5KDA3_CRYNJ Q5KDA3_CRYNJ Q5KDB1_CRYNJ Q5KDB1_CRYNJ Q5KDM0_CRYNJ Q5KDM0_CRYNJ Q5KDT1_CRYNJ Q5KDT1_CRYNJ Q5KDU1_CRYNJ Q5KDU1_CRYNJ Q5KDU2_CRYNJ Q5KDU2_CRYNJ Q5KDU5_CRYNJ Q5KDU5_CRYNJ Q5KDU9_CRYNJ Q5KDU9_CRYNJ Q5KDW0_CRYNJ Q5KDW0_CRYNJ Q5KE76_CRYNJ Q5KE76_CRYNJ Q5KE79_CRYNJ Q5KE79_CRYNJ Q5KEA9_CRYNJ Q5KEA9_CRYNJ Q5KED1_CRYNJ Q5KED1_CRYNJ Q5KEF7_CRYNJ Q5KEF7_CRYNJ Q5KEH2_CRYNJ Q5KEH2_CRYNJ Q5KQ38_CRYNJ Q5KQ38_CRYNJ Q5KEH7_CRYNJ Q5KEH7_CRYNJ Q5KEN2_CRYNJ Q5KEN2_CRYNJ Q5KEQ0_CRYNJ Q5KEQ0_CRYNJ Q5KEW4_CRYNJ Q5KEW4_CRYNJ Q5KEX5_CRYNJ Q5KEX5_CRYNJ Q5KEZ5_CRYNJ Q5KEZ5_CRYNJ Q5KEZ7_CRYNJ Q5KEZ7_CRYNJ Q5KF04_CRYNJ Q5KF04_CRYNJ Q5KF23_CRYNJ Q5KF23_CRYNJ Q5KF63_CRYNJ Q5KF63_CRYNJ Q5KF78_CRYNJ Q5KF78_CRYNJ Q5KFA1_CRYNJ Q5KFA1_CRYNJ Q5KFB9_CRYNJ Q5KFB9_CRYNJ Q5KFE4_CRYNJ Q5KFE4_CRYNJ Q5KFF8_CRYNJ Q5KFF8_CRYNJ Q5KFH7_CRYNJ Q5KFH7_CRYNJ Q5KFL3_CRYNJ Q5KFL3_CRYNJ Q5KFL5_CRYNJ Q5KFL5_CRYNJ Q5KFS7_CRYNJ Q5KFS7_CRYNJ Q5KFT4_CRYNJ Q5KFT4_CRYNJ Q5KFU0_CRYNJ Q5KFU0_CRYNJ Q5KFX3_CRYNJ Q5KFX3_CRYNJ Q5KG39_CRYNJ Q5KG39_CRYNJ Q5KG89_CRYNJ Q5KG89_CRYNJ Q5KGB2_CRYNJ Q5KGB2_CRYNJ Q5KGD9_CRYNJ Q5KGD9_CRYNJ Q5KGN1_CRYNJ Q5KGN1_CRYNJ Q5KGP7_CRYNJ Q5KGP7_CRYNJ Q5KGU5_CRYNJ Q5KGU5_CRYNJ Q5KGV5_CRYNJ Q5KGV5_CRYNJ Q5KGZ9_CRYNJ Q5KGZ9_CRYNJ Q5KH01_CRYNJ Q5KH01_CRYNJ Q5KH85_CRYNJ Q5KH85_CRYNJ Q5KHA1_CRYNJ Q5KHA1_CRYNJ Q5KHC9_CRYNJ Q5KHC9_CRYNJ Q5KHT1_CRYNJ Q5KHT1_CRYNJ Q5KHT8_CRYNJ Q5KHT8_CRYNJ Q5KHU7_CRYNJ Q5KHU7_CRYNJ Q5KHW4_CRYNJ Q5KHW4_CRYNJ Q5KI28_CRYNJ Q5KI28_CRYNJ Q5KI75_CRYNJ Q5KI75_CRYNJ Q5KI86_CRYNJ Q5KI86_CRYNJ Q5KIA5_CRYNJ Q5KIA5_CRYNJ Q5KID6_CRYNJ Q5KID6_CRYNJ Q5KID7_CRYNJ Q5KID7_CRYNJ Q5KID8_CRYNJ Q5KID8_CRYNJ Q5KIE2_CRYNJ Q5KIE2_CRYNJ Q5KIF5_CRYNJ Q5KIF5_CRYNJ Q5KIM9_CRYNJ Q5KIM9_CRYNJ Q5KIN5_CRYNJ Q5KIN5_CRYNJ Q5KIN6_CRYNJ Q5KIN6_CRYNJ Q5KIV8_CRYNJ Q5KIV8_CRYNJ Q5KIW2_CRYNJ Q5KIW2_CRYNJ Q5KIZ0_CRYNJ Q5KIZ0_CRYNJ Q5KIZ1_CRYNJ Q5KIZ1_CRYNJ Q5KIZ7_CRYNJ Q5KIZ7_CRYNJ Q5KJ79_CRYNJ Q5KJ79_CRYNJ Q5KJC6_CRYNJ Q5KJC6_CRYNJ Q5KJD9_CRYNJ Q5KJD9_CRYNJ Q5KJG1_CRYNJ Q5KJG1_CRYNJ Q5KJI7_CRYNJ Q5KJI7_CRYNJ Q5KJJ6_CRYNJ Q5KJJ6_CRYNJ Q5KJJ9_CRYNJ Q5KJJ9_CRYNJ Q5KJP2_CRYNJ Q5KJP2_CRYNJ Q5KJQ3_CRYNJ Q5KJQ3_CRYNJ Q5KJQ5_CRYNJ Q5KJQ5_CRYNJ Q5KJQ6_CRYNJ Q5KJQ6_CRYNJ Q5KJT0_CRYNJ Q5KJT0_CRYNJ Q5KJT1_CRYNJ Q5KJT1_CRYNJ Q5KJV2_CRYNJ Q5KJV2_CRYNJ Q5KJW3_CRYNJ Q5KJW3_CRYNJ Q5KJZ1_CRYNJ Q5KJZ1_CRYNJ Q5KK05_CRYNJ Q5KK05_CRYNJ Q5KK91_CRYNJ Q5KK91_CRYNJ Q5KKE9_CRYNJ Q5KKE9_CRYNJ Q5KKG9_CRYNJ Q5KKG9_CRYNJ Q5KKI3_CRYNJ Q5KKI3_CRYNJ Q5KKK1_CRYNJ Q5KKK1_CRYNJ Q5KKS9_CRYNJ Q5KKS9_CRYNJ Q5KKW7_CRYNJ Q5KKW7_CRYNJ Q5KKX0_CRYNJ Q5KKX0_CRYNJ Q5KL04_CRYNJ Q5KL04_CRYNJ Q5KL26_CRYNJ Q5KL26_CRYNJ Q5KL41_CRYNJ Q5KL41_CRYNJ Q5KL66_CRYNJ Q5KL66_CRYNJ Q5KLD3_CRYNJ Q5KLD3_CRYNJ Q5KLE1_CRYNJ Q5KLE1_CRYNJ Q5KLE4_CRYNJ Q5KLE4_CRYNJ Q5KLI4_CRYNJ Q5KLI4_CRYNJ Q5KLP2_CRYNJ Q5KLP2_CRYNJ Q5KLS9_CRYNJ Q5KLS9_CRYNJ Q5KLT1_CRYNJ Q5KLT1_CRYNJ Q5KLT4_CRYNJ Q5KLT4_CRYNJ Q5KLY0_CRYNJ Q5KLY0_CRYNJ Q5KLZ6_CRYNJ Q5KLZ6_CRYNJ Q5KM37_CRYNJ Q5KM37_CRYNJ Q5KPZ9_CRYNJ Q5KPZ9_CRYNJ Q5KM59_CRYNJ Q5KM59_CRYNJ Q5KMF5_CRYNJ Q5KMF5_CRYNJ Q5KMH4_CRYNJ Q5KMH4_CRYNJ Q5KMJ1_CRYNJ Q5KMJ1_CRYNJ Q5KMK2_CRYNJ Q5KMK2_CRYNJ Q5KMN4_CRYNJ Q5KMN4_CRYNJ Q5KMQ0_CRYNJ Q5KMQ0_CRYNJ Q5KMR1_CRYNJ Q5KMR1_CRYNJ Q5KMR4_CRYNJ Q5KMR4_CRYNJ Q5KMS5_CRYNJ Q5KMS5_CRYNJ Q5KMV9_CRYNJ Q5KMV9_CRYNJ Q5KMY1_CRYNJ Q5KMY1_CRYNJ Q5KMZ4_CRYNJ Q5KMZ4_CRYNJ Q5KN99_CRYNJ Q5KN99_CRYNJ Q5KNA1_CRYNJ Q5KNA1_CRYNJ Q5KNC8_CRYNJ Q5KNC8_CRYNJ Q5KND0_CRYNJ Q5KND0_CRYNJ Q5KNG8_CRYNJ Q5KNG8_CRYNJ Q5KPS8_CRYNJ Q5KPS8_CRYNJ Q5KNJ1_CRYNJ Q5KNJ1_CRYNJ Q5KNL8_CRYNJ Q5KNL8_CRYNJ Q5KNR5_CRYNJ Q5KNR5_CRYNJ Q5KNT0_CRYNJ Q5KNT0_CRYNJ Q5KNV4_CRYNJ Q5KNV4_CRYNJ Q5KNV6_CRYNJ Q5KNV6_CRYNJ Q5KNY1_CRYNJ Q5KNY1_CRYNJ Q5KP16_CRYNJ Q5KP16_CRYNJ Q5KP19_CRYNJ Q5KP19_CRYNJ Q5KP23_CRYNJ Q5KP23_CRYNJ Q5KP39_CRYNJ Q5KP39_CRYNJ Q5KP61_CRYNJ Q5KP61_CRYNJ Q5KP79_CRYNJ Q5KP79_CRYNJ Q5KPA4_CRYNJ Q5KPA4_CRYNJ Q5KPD4_CRYNJ Q5KPD4_CRYNJ Q5KQ15_CRYNJ Q5KQ15_CRYNJ Q5KPE2_CRYNJ Q5KPE2_CRYNJ Q5KPF8_CRYNJ Q5KPF8_CRYNJ Q5KPI4_CRYNJ Q5KPI4_CRYNJ Q5KPJ0_CRYNJ Q5KPJ0_CRYNJ Q5KPL4_CRYNJ Q5KPL4_CRYNJ Q5KPM7_CRYNJ Q5KPM7_CRYNJ
Nodes:
Network nodes represent proteins
splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
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colored nodes:
query proteins and first shell of interactors
white nodes:
second shell of interactors
Node Content
empty nodes:
proteins of unknown 3D structure
filled nodes:
a 3D structure is known or predicted
Edges:
Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding to each other.
Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
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textmining
co-expression
protein homology
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Q5KPQ9_CRYNJAP-1 complex subunit gamma. (854 aa)
Q5KPR9_CRYNJER membrane protein complex subunit 4; Belongs to the EMC4 family. (197 aa)
Q5KPS5_CRYNJVacuolar protein sorting-associated protein 29; Belongs to the VPS29 family. (203 aa)
A0A0S2LHW3Uncharacterized protein. (52 aa)
A0A0S2LI43Uncharacterized protein. (326 aa)
A0A0S2LII0Uncharacterized protein. (90 aa)
A0A0S2LIJ5Uncharacterized protein. (226 aa)
A0A0S2LIL8Uncharacterized protein. (143 aa)
A0A0S2LIR2Uncharacterized protein. (336 aa)
A0A0S2LIT1FCP1 homology domain-containing protein. (495 aa)
A0A0S2LIX3Uncharacterized protein. (206 aa)
A0A0S2LIY7V-SNARE coiled-coil homology domain-containing protein. (154 aa)
A0A0S2M5A9G protein gamma domain-containing protein. (87 aa)
A0A0S2M5L1Uncharacterized protein. (220 aa)
A0A0S2M5R0Uncharacterized protein. (208 aa)
A0A0S2M5Z0G protein gamma domain-containing protein. (81 aa)
A0A0S2M611Uncharacterized protein. (293 aa)
A0A0S2M691Ubiquitin-like domain-containing protein. (511 aa)
ALG14UDP-N-acetylglucosamine transferase subunit ALG14; Involved in protein N-glycosylation. Essential for the second step of the dolichol-linked oligosaccharide pathway. Anchors the catalytic subunit ALG13 to the ER (By similarity). (229 aa)
CYN1Cyanate hydratase; Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide; Belongs to the cyanase family. (183 aa)
TIM50Mitochondrial import inner membrane translocase subunit TIM50; Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane. Required to direct preproteins in transit and direct them to the channel protein TIM23, and possibly facilitates transfer of the translocating proteins from the TOM complex to the TIM23 complex (By similarity). (516 aa)
GPA1Guanine nucleotide-binding protein subunit alpha; Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. Involved in the mating pathway; Belongs to the G-alpha family. (432 aa)
MDM10Mitochondrial distribution and morphology protein 10; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis and may function in phospholipid exchange. MDM10 is involved in the late assembly steps of the general translocase of the mitochondrial outer membrane (TOM complex). Functions in the TOM40-specific route of the assembly of outer membrane beta-barrel proteins, including the association of TOM40 with the recepto [...] (508 aa)
MDM12Mitochondrial distribution and morphology protein 12; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. MDM12 is required for the interaction of the ER-resident membrane protein MMM1 and the outer mitochondrial membrane-resident beta-barrel protein MDM10. The MDM12-MMM1 subcomplex functions in the major beta-barrel assembly pat [...] (388 aa)
MDM34Mitochondrial distribution and morphology protein 34; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. MDM34 is required for the interaction of the ER-resident membrane protein MMM1 and the outer mitochondrial membrane-resident beta-barrel protein MDM10. (343 aa)
MMM1Maintenance of mitochondrial morphology protein 1; Component of the ERMES/MDM complex, which serves as a molecular tether to connect the endoplasmic reticulum (ER) and mitochondria. Components of this complex are involved in the control of mitochondrial shape and protein biogenesis, and function in nonvesicular lipid trafficking between the ER and mitochondria. The MDM12-MMM1 subcomplex functions in the major beta-barrel assembly pathway that is responsible for biogenesis of all outer membrane beta- barrel proteins, and acts in a late step after the SAM complex. The MDM10-MDM12-MMM1 su [...] (475 aa)
NPL4Nuclear protein localization protein 4; Involved in the import of nuclear-targeted proteins into the nucleus and the export of poly(A) RNA out of the nucleus. Has a role in the endoplasmic reticulum-associated degradation (ERAD) pathway (By similarity); Belongs to the NPL4 family. (693 aa)
PAM17Presequence translocated-associated motor subunit PAM17, mitochondrial; Component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. (217 aa)
SAR1Small COPII coat GTPase SAR1; Small GTPase component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules. SAR1 controls the coat assembly in a stepwise manner. Activated SAR1-GTP binds to membranes first and recruits the SEC23/24 complex. These SEC23/24-SAR1 prebudding intermediates are then collected by the SEC13/31 complex as subunits polymerize to form coated trans [...] (189 aa)
SEC23Protein transport protein SEC23; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules (By similarity). (763 aa)
SEC24Protein transport protein SEC24; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules (By similarity); Belongs to the SEC23/SEC24 family. SEC24 subfamily. (920 aa)
SNF7Vacuolar-sorting protein SNF7; Required for the sorting and concentration of proteins resulting in the entry of these proteins into the invaginating vesicles of the multivesicular body (MVB). Also required for the proteolytic cleavage of the transcription factor RIM101 in response to alkaline ambient pH (By similarity). (220 aa)
SNX3Sorting nexin-3; Required for retention of late Golgi membrane proteins. Component of the retrieval machinery that functions by direct interaction with the cytosolic tails of certain TGN membrane proteins during the sorting/budding process at the prevacuolar compartment. Binds phosphatidylinositol 3-phosphate (PtdIns(P3)) (By similarity). (144 aa)
TIM22Mitochondrial import inner membrane translocase subunit TIM22; Essential core component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. In the TIM22 complex, it constitutes the voltage-activated and signal-gated channel. Forms a twin-pore translocase that uses the membrane potential as external driving force in 2 voltage-dependent steps (By similarity). (187 aa)
TIM54Mitochondrial import inner membrane translocase subunit TIM54; Essential component of the TIM22 complex, a complex that mediates the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. The TIM22 complex forms a twin- pore translocase that uses the membrane potential as external driving force (By similarity). (458 aa)
TIM9Mitochondrial import inner membrane translocase subunit TIM9; Mitochondrial intermembrane chaperone that participates in the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. Also required for the transfer of beta- barrel precursors from the TOM complex to the sorting and assembly machinery (SAM complex) of the outer membrane. Acts as a chaperone-like protein that protects the hydrophobic precursors from aggregation and guide them through the mitochondrial intermembrane space (By similarity); Belongs to the small Tim family. (89 aa)
TIM10Mitochondrial import inner membrane translocase subunit TIM10; Mitochondrial intermembrane chaperone that participates in the import and insertion of multi-pass transmembrane proteins into the mitochondrial inner membrane. Also required for the transfer of beta- barrel precursors from the TOM complex to the sorting and assembly machinery (SAM complex) of the outer membrane. Acts as a chaperone-like protein that protects the hydrophobic precursors from aggregation and guide them through the mitochondrial intermembrane space (By similarity); Belongs to the small Tim family. (102 aa)
SEC13Protein transport protein SEC13; Component of the coat protein complex II (COPII) which promotes the formation of transport vesicles from the endoplasmic reticulum (ER). The coat has two main functions, the physical deformation of the endoplasmic reticulum membrane into vesicles and the selection of cargo molecules. It also functions as a component of the nuclear pore complex (NPC). NPC components, collectively referred to as nucleoporins (NUPs), can play the role of both NPC structural components and of docking or interaction partners for transiently associated nuclear transport facto [...] (339 aa)
Q5K6T7_CRYNJ1,3-beta-glucan synthase, putative. (1801 aa)
Q5K6T9_CRYNJExpressed protein. (475 aa)
Q5K6Y2_CRYNJResponse to unfolded-protein, putative. (277 aa)
Q5K6Z4_CRYNJSignal peptidase subunit 3. (199 aa)
Q5K701_CRYNJMICOS complex subunit MIC10; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (99 aa)
Q5K720_CRYNJAP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (143 aa)
Q5K728_CRYNJExpressed protein. (71 aa)
Q5K757_CRYNJE3 ubiquitin-protein ligase PEP5. (1071 aa)
Q5K779_CRYNJProtein transport protein Sec61 subunit beta; Necessary for protein translocation in the endoplasmic reticulum. (100 aa)
Q5K7H4_CRYNJUncharacterized protein. (441 aa)
Q5K7H5_CRYNJAcidic laccase, putative; Belongs to the multicopper oxidase family. (640 aa)
Q5K7J0_CRYNJUncharacterized protein. (131 aa)
Q5K7M2_CRYNJt-SNARE coiled-coil homology domain-containing protein. (356 aa)
Q5K7N6_CRYNJUncharacterized protein. (179 aa)
Q5K7Q5_CRYNJPIPK domain-containing protein. (1821 aa)
Q5K7S8_CRYNJzf-CHCC domain-containing protein. (144 aa)
Q5K7X0_CRYNJER to Golgi transport-related protein, putative. (1003 aa)
Q5K7Z1_CRYNJExpressed protein. (682 aa)
Q5K822_CRYNJExpressed protein. (531 aa)
Q5K888_CRYNJUbiquitin fusion-degradation 1-like protein, putative. (481 aa)
Q5K889_CRYNJt-SNARE, putative; Belongs to the syntaxin family. (409 aa)
Q5K8G6_CRYNJUncharacterized protein. (235 aa)
Q5K8H0_CRYNJUncharacterized protein. (114 aa)
Q5K8J0_CRYNJExpressed protein. (74 aa)
Q5K8K8_CRYNJMICOS complex subunit MIC60; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (725 aa)
Q5K8L7_CRYNJENTH domain-containing protein. (494 aa)
Q5K8Q1_CRYNJCytochrome c oxidase polypeptide iv, mitochondrial, putative. (158 aa)
VMA9V-type proton ATPase subunit e; Subunit of the integral membrane V0 complex of vacuolar ATPase (By similarity). V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (71 aa)
Q5K8T1_CRYNJExpressed protein. (312 aa)
Q5K8U4_CRYNJUbiquinol-cytochrome C reductase complex core protein 2, putative. (434 aa)
Q5K8W3_CRYNJNADH-ubiquinone oxidoreductase; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (155 aa)
Q5K8Y5_CRYNJUncharacterized protein. (435 aa)
Q5K906_CRYNJAP complex subunit beta; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (755 aa)
Q5K938_CRYNJV-type proton ATPase proteolipid subunit; Proton-conducting pore forming subunit of the membrane integral V0 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (167 aa)
Q5K946_CRYNJCytochrome c oxidase subunit V, putative. (167 aa)
Q5K9E5_CRYNJGrpe protein, putative; Belongs to the GrpE family. (228 aa)
Q5K9H6_CRYNJChloride channel protein. (864 aa)
Q5K9K1_CRYNJUncharacterized protein. (1535 aa)
Q5K9K5_CRYNJUncharacterized protein. (361 aa)
Q5K9Y4_CRYNJUDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase, putative. (502 aa)
Q5KA21_CRYNJIntegral membrane protein sed5, putative. (364 aa)
Q5KA29_CRYNJClathrin heavy chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin heavy chain family. (1684 aa)
Q5KA71_CRYNJMMS2, putative; Belongs to the AAA ATPase family. (810 aa)
Q5KA77_CRYNJMitochondrial import receptor subunit tom22, putative. (149 aa)
Q5KAA7_CRYNJHydrogen-transporting ATPase, putative; Belongs to the V-ATPase proteolipid subunit family. (198 aa)
Q5KAB5_CRYNJStructural molecule, putative. (1440 aa)
Q5KAG9_CRYNJDolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit WBP1; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the [...] (468 aa)
Q5KAJ6_CRYNJDolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the en [...] (480 aa)
Q5KAU1_CRYNJUncharacterized protein. (181 aa)
Q5KAX9_CRYNJFerro-O2-oxidoreductase, putative; Belongs to the multicopper oxidase family. (632 aa)
Q5KB19_CRYNJSNAP receptor, putative. (269 aa)
Q5KB78_CRYNJVoltage-gated potassium channel beta-2 subunit, putative. (355 aa)
Q5KBA0_CRYNJSuccinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial; Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (637 aa)
Q5KBG5_CRYNJMitochondrial import inner membrane translocase subunit tim17, putative. (161 aa)
Q5KBG8_CRYNJExpressed protein. (72 aa)
Q5KBH1_CRYNJVacuolar protein sorting-associated protein 41; Required for vacuolar assembly and vacuolar traffic. Belongs to the VPS41 family. (1038 aa)
Q5KBI9_CRYNJExpressed protein. (518 aa)
Q5KBP6_CRYNJLRRNT_2 domain-containing protein. (840 aa)
Q5KBP7_CRYNJUncharacterized protein. (821 aa)
Q5KBR2_CRYNJUncharacterized protein. (123 aa)
Q5KBR3_CRYNJTrafficking-related protein, putative. (130 aa)
Q5KBW0_CRYNJVacuolar proton pump subunit B; Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase; Belongs to the ATPase alpha/beta chains family. (515 aa)
Q5KC20_CRYNJClathrin light chain; Clathrin is the major protein of the polyhedral coat of coated pits and vesicles; Belongs to the clathrin light chain family. (288 aa)
Q5KC44_CRYNJGPI-anchor transamidase, putative. (553 aa)
Q5KC66_CRYNJExpressed protein. (408 aa)
Q5KC69_CRYNJProtein transporter, putative. (478 aa)
Q5KCD5_CRYNJRab guanyl-nucleotide exchange factor, putative. (570 aa)
Q5KCF2_CRYNJGPI anchor biosynthesis-related protein, putative. (534 aa)
Q5KCH4_CRYNJNADH dehydrogenase 10.5K chain, putative. (100 aa)
Q5KCK0_CRYNJRING-type domain-containing protein. (740 aa)
Q5KCK9_CRYNJUncharacterized protein. (251 aa)
Q5KCR0_CRYNJExpressed protein. (236 aa)
Q5KCT8_CRYNJUncharacterized protein. (346 aa)
Q5KCX6_CRYNJSyntaxin, putative. (352 aa)
Q5KCZ2_CRYNJNADH-ubiquinone oxidoreductase, putative; Belongs to the complex I 49 kDa subunit family. (452 aa)
Q5KCZ3_CRYNJUbiquinol-cytochrome c reductase complex 7.3 kDa protein, putative. (66 aa)
Q5KD38_CRYNJARF GTPase activator, putative. (479 aa)
Q5KD54_CRYNJUncharacterized protein. (289 aa)
Q5KD71_CRYNJV-SNARE, putative. (120 aa)
Q5KDA3_CRYNJAP complex subunit beta; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (755 aa)
Q5KDB1_CRYNJUncharacterized protein. (167 aa)
Q5KDM0_CRYNJSuccinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial; Iron-sulfur protein (IP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q). (289 aa)
Q5KDT1_CRYNJGolgi SNAP receptor complex member 1; Involved in transport from the ER to the Golgi apparatus as well as in intra-Golgi transport. It belongs to a super-family of proteins called t-SNAREs or soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein receptor. (238 aa)
Q5KDU1_CRYNJExpressed protein. (90 aa)
Q5KDU2_CRYNJCoatomer subunit beta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (952 aa)
Q5KDU5_CRYNJCytoplasm protein, putative. (604 aa)
Q5KDU9_CRYNJt-SNARE coiled-coil homology domain-containing protein. (229 aa)
Q5KDW0_CRYNJClathrin assembly protein AP47, putative; Belongs to the adaptor complexes medium subunit family. (435 aa)
Q5KE76_CRYNJUncharacterized protein. (216 aa)
Q5KE79_CRYNJUncharacterized protein. (573 aa)
Q5KEA9_CRYNJUncharacterized protein. (1214 aa)
Q5KED1_CRYNJOsmosensor, putative. (1883 aa)
Q5KEF7_CRYNJAP-2 complex subunit alpha; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (1047 aa)
Q5KEH2_CRYNJUncharacterized protein. (170 aa)
Q5KQ38_CRYNJUncharacterized protein. (70 aa)
Q5KEH7_CRYNJCoatomer subunit alpha; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. (1222 aa)
Q5KEN2_CRYNJAdaptin_N domain-containing protein. (859 aa)
Q5KEQ0_CRYNJEndoplasmic reticulum protein, putative. (1022 aa)
Q5KEW4_CRYNJMitochondrion protein, putative. (566 aa)
Q5KEX5_CRYNJMitochondrial import inner membrane translocase subunit TIM44; Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner; Belongs to the Tim44 family. (454 aa)
Q5KEZ5_CRYNJGPI-anchor transamidase; Mediates GPI anchoring in the endoplasmic reticulum, by replacing a protein's C-terminal GPI attachment signal peptide with a pre-assembled GPI. During this transamidation reaction, the GPI transamidase forms a carbonyl intermediate with the substrate protein. Belongs to the peptidase C13 family. (415 aa)
Q5KEZ7_CRYNJUncharacterized protein. (268 aa)
Q5KF04_CRYNJUCR_hinge domain-containing protein. (126 aa)
Q5KF23_CRYNJNADH-ubiquinone oxidoreductase 30.4 kDa subunit, putative; Belongs to the complex I 30 kDa subunit family. (270 aa)
Q5KF63_CRYNJV-type proton ATPase subunit F; Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (121 aa)
Q5KF78_CRYNJNegative regulation of transcription by glucose-related protein, putative. (275 aa)
Q5KFA1_CRYNJER membrane protein complex subunit 3; The EMC seems to be required for efficient folding of proteins in the endoplasmic reticulum (ER). Belongs to the EMC3 family. (270 aa)
Q5KFB9_CRYNJATP synthase subunit alpha; Produces ATP from ADP in the presence of a proton gradient across the membrane. (540 aa)
Q5KFE4_CRYNJUncharacterized protein. (663 aa)
Q5KFF8_CRYNJV-type proton ATPase subunit G; Catalytic subunit of the peripheral V1 complex of vacuolar ATPase (V-ATPase). V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (119 aa)
Q5KFH7_CRYNJt-SNARE coiled-coil homology domain-containing protein. (392 aa)
Q5KFL3_CRYNJNAD_binding_2 domain-containing protein. (312 aa)
Q5KFL5_CRYNJCytochrome c oxidase subunit; This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport. (82 aa)
Q5KFS7_CRYNJAP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (220 aa)
Q5KFT4_CRYNJElectron transporter, transferring electrons within CoQH2-cytochrome c reductase complex, putative. (320 aa)
Q5KFU0_CRYNJATP synthase subunit beta; Produces ATP from ADP in the presence of a proton gradient across the membrane. (547 aa)
Q5KFX3_CRYNJUAS domain-containing protein. (567 aa)
Q5KG39_CRYNJJ domain-containing protein. (615 aa)
Q5KG89_CRYNJHeterotrimeric G-protein GTPase, putative. (358 aa)
Q5KGB2_CRYNJAP complex subunit sigma; Belongs to the adaptor complexes small subunit family. (164 aa)
Q5KGD9_CRYNJNADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit; Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. (144 aa)
Q5KGN1_CRYNJUbiquitin conjugating enzyme, putative; Belongs to the ubiquitin-conjugating enzyme family. (175 aa)
Q5KGP7_CRYNJOxidored_q6 domain-containing protein; Belongs to the complex I 20 kDa subunit family. (229 aa)
Q5KGU5_CRYNJCytochrome b-c1 complex subunit Rieske, mitochondrial; Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis. (279 aa)
Q5KGV5_CRYNJEndodeoxyribonuclease, putative. (618 aa)
Q5KGZ9_CRYNJATP binding protein, putative; Belongs to the STXBP/unc-18/SEC1 family. (672 aa)
Q5KH01_CRYNJPolyphosphoinositide phosphatase, putative. (827 aa)
Q5KH85_CRYNJAP-3 complex subunit delta; Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane. (939 aa)
Q5KHA1_CRYNJATP synthase subunit gamma. (288 aa)
Q5KHC9_CRYNJExpressed protein. (325 aa)
Q5KHT1_CRYNJProtein-Golgi retention-related protein, putative. (295 aa)
Q5KHT8_CRYNJExpressed protein. (314 aa)
Q5KHU7_CRYNJCoatomer subunit delta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (259 aa)
Q5KHW4_CRYNJMitochondrial import inner membrane translocase subunit tim23, putative. (241 aa)
Q5KI28_CRYNJUbiquinol-cytochrome-c reductase, putative. (166 aa)
Q5KI75_CRYNJCoatomer subunit gamma; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (921 aa)
Q5KI86_CRYNJWD_REPEATS_REGION domain-containing protein. (343 aa)
Q5KIA5_CRYNJUncharacterized protein. (1021 aa)
Q5KID6_CRYNJCoatomer subunit epsilon; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. The coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. Belongs to the COPE family. (306 aa)
Q5KID7_CRYNJ1-phosphatidylinositol-3-phosphate 5-kinase, putative. (2432 aa)
Q5KID8_CRYNJUncharacterized protein. (2102 aa)
Q5KIE2_CRYNJUncharacterized protein. (208 aa)
Q5KIF5_CRYNJUncharacterized protein; Belongs to the synaptobrevin family. (224 aa)
Q5KIM9_CRYNJUncharacterized protein. (106 aa)
Q5KIN5_CRYNJ1-acyl-sn-glycerol-3-phosphate acyltransferase; Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family. (783 aa)
Q5KIN6_CRYNJV-type proton ATPase subunit a; Essential component of the vacuolar proton pump (V-ATPase), a multimeric enzyme that catalyzes the translocation of protons across the membranes. Required for assembly and activity of the V-ATPase. (849 aa)
Q5KIV8_CRYNJt-SNARE coiled-coil homology domain-containing protein. (257 aa)
Q5KIW2_CRYNJUncharacterized protein. (250 aa)
Q5KIZ0_CRYNJUncharacterized protein. (61 aa)
Q5KIZ1_CRYNJDolichyl-phosphate-mannose-protein mannosyltransferase, putative. (767 aa)
Q5KIZ7_CRYNJUncharacterized protein. (122 aa)
Q5KJ79_CRYNJExpressed protein. (73 aa)
Q5KJC6_CRYNJUncharacterized protein. (697 aa)
Q5KJD9_CRYNJExpressed protein. (385 aa)
Q5KJG1_CRYNJV-type proton ATPase subunit C; Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit C is necessary for the assembly of the catalytic sector of the enzyme and is likely to have a specific function in its catalytic activity. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (396 aa)
Q5KJI7_CRYNJGolgi to vacuole transport-related protein, putative. (849 aa)
Q5KJJ6_CRYNJBET1 protein, putative. (155 aa)
Q5KJJ9_CRYNJCytoplasm protein, putative. (654 aa)
Q5KJP2_CRYNJVoltage-dependent ion-selective channel, putative. (292 aa)
Q5KJQ3_CRYNJExpressed protein. (60 aa)
Q5KJQ5_CRYNJHigh-affinity iron permease CaFTR1, putative. (433 aa)
Q5KJQ6_CRYNJFerroxidase, putative; Belongs to the multicopper oxidase family. (639 aa)
Q5KJT0_CRYNJX15341 cytochrome C oxidase subunit, putative; Belongs to the cytochrome c oxidase subunit 6A family. (119 aa)
Q5KJT1_CRYNJJ domain-containing protein. (717 aa)
Q5KJV2_CRYNJHydrogen-transporting ATP synthase, putative. (100 aa)
Q5KJW3_CRYNJUncharacterized protein. (121 aa)
Q5KJZ1_CRYNJMitochondrial inner membrane protease subunit. (222 aa)
Q5KK05_CRYNJDolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the en [...] (297 aa)
Q5KK91_CRYNJUncharacterized protein. (156 aa)
Q5KKE9_CRYNJVacuolar protein sorting-associated protein 35; Plays a role in vesicular protein sorting. (938 aa)
Q5KKG9_CRYNJSignal recognition particle binding protein, putative. (674 aa)
Q5KKI3_CRYNJUncharacterized protein. (119 aa)
Q5KKK1_CRYNJUncharacterized protein. (532 aa)
Q5KKS9_CRYNJATP-dependent peptidase, putative. (782 aa)
Q5KKW7_CRYNJUncharacterized protein. (175 aa)
Q5KKX0_CRYNJExpressed protein. (302 aa)
Q5KL04_CRYNJDigA protein, putative. (1177 aa)
Q5KL26_CRYNJATP synthase, putative. (237 aa)
Q5KL41_CRYNJExpressed protein. (347 aa)
Q5KL66_CRYNJVacuolar ATP synthase subunit d, putative. (263 aa)
Q5KLD3_CRYNJCoatomer subunit zeta; The zeta subunit may be involved in regulating the coat assembly and, hence, the rate of biosynthetic protein transport due to its association-dissociation properties with the coatomer complex. (223 aa)
Q5KLE1_CRYNJDolichyl-diphosphooligosaccharide-protein glycotransferase, putative. (322 aa)
Q5KLE4_CRYNJCoatomer subunit beta; The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin- coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. (829 aa)
Q5KLI4_CRYNJATPase, putative. (817 aa)
Q5KLP2_CRYNJATP synthase subunit d, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the cent [...] (173 aa)
Q5KLS9_CRYNJMitochondrial import receptor subunit tom40, putative. (375 aa)
Q5KLT1_CRYNJAP complex subunit beta; Adaptins are components of the adaptor complexes which link clathrin to receptors in coated vesicles. Clathrin-associated protein complexes are believed to interact with the cytoplasmic tails of membrane proteins, leading to their selection and concentration. (696 aa)
Q5KLT4_CRYNJPeptidase, putative. (182 aa)
Q5KLY0_CRYNJAdaptor complex subunit medium chain 3, putative; Belongs to the adaptor complexes medium subunit family. (454 aa)
Q5KLZ6_CRYNJCytochrome-c oxidase chain VI, putative. (142 aa)
Q5KM37_CRYNJPhosphatidylinositol 3-kinase VPS34. (880 aa)
Q5KPZ9_CRYNJMCU domain-containing protein. (556 aa)
Q5KM59_CRYNJExpressed protein. (395 aa)
Q5KMF5_CRYNJIntracellular protein transport-related protein, putative; Belongs to the adaptor complexes medium subunit family. (428 aa)
Q5KMH4_CRYNJProtein kinase/endoribonuclease, putative. (1073 aa)
Q5KMJ1_CRYNJt-SNARE, putative; Belongs to the syntaxin family. (274 aa)
Q5KMK2_CRYNJExpressed protein. (379 aa)
Q5KMN4_CRYNJIon_trans domain-containing protein. (554 aa)
Q5KMQ0_CRYNJUncharacterized protein. (335 aa)
Q5KMR1_CRYNJSuccinate dehydrogenase [ubiquinone] cytochrome b small subunit. (181 aa)
Q5KMR4_CRYNJUncharacterized protein. (835 aa)
Q5KMS5_CRYNJProbable vacuolar protein sorting-associated protein 16 homolog; Essential for vacuolar protein sorting. Required for vacuole biogenesis, stability and to maintain vacuole morphology. (847 aa)
Q5KMV9_CRYNJATP synthase delta chain, mitochondrial, putative. (168 aa)
Q5KMY1_CRYNJProtein-vacuolar targeting-related protein, putative. (187 aa)
Q5KMZ4_CRYNJLigase, putative. (852 aa)
Q5KN99_CRYNJAlpha-1,6-mannosyltransferase, putative. (572 aa)
Q5KNA1_CRYNJSerine C-palmitoyltransferase, putative. (526 aa)
Q5KNC8_CRYNJUncharacterized protein. (80 aa)
Q5KND0_CRYNJV-type proton ATPase subunit H; Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit H activates ATPase activity of the enzyme and couples ATPase activity to proton flow. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system. (444 aa)
Q5KNG8_CRYNJVacuolar protein sorting-associated protein 28; Component of the ESCRT-I complex (endosomal sorting complex required for transport I), a regulator of vesicular trafficking process. (213 aa)
Q5KPS8_CRYNJHeterotrimeric G protein alpha subunit B, putative. (352 aa)
Q5KNJ1_CRYNJATP-binding cassette (ABC) transporter, putative. (853 aa)
Q5KNL8_CRYNJUncharacterized protein. (283 aa)
Q5KNR5_CRYNJUncharacterized protein. (131 aa)
Q5KNT0_CRYNJVacuolar ATP synthase subunit e, putative. (227 aa)
Q5KNV4_CRYNJExpressed protein. (85 aa)
Q5KNV6_CRYNJExpressed protein. (76 aa)
Q5KNY1_CRYNJRetrograde transport, endosome to Golgi-related protein, putative. (817 aa)
Q5KP16_CRYNJDolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit OST2; Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol- pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the [...] (123 aa)
Q5KP19_CRYNJProtein-vacuolar targeting-related protein, putative. (202 aa)
Q5KP23_CRYNJDUF1681 domain-containing protein. (200 aa)
Q5KP39_CRYNJV-type proton ATPase subunit; Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. The active enzyme consists of a catalytic V1 domain attached to an integral membrane V0 proton pore complex. This subunit is a non-integral membrane component of the membrane pore domain and is required for proper assembly of the V0 sector. Might be involved in the regulated assembly of V1 subunits onto the membrane sector or alternatively may prevent the passage of protons through V0 pores; Belongs to the V-ATPase V0D/AC39 subunit family. (356 aa)
Q5KP61_CRYNJLate endosome to vacuole transport-related protein, putative. (212 aa)
Q5KP79_CRYNJCell division cycle protein 91, putative. (436 aa)
Q5KPA4_CRYNJSuccinate dehydrogenase (Ubiquinone), putative. (177 aa)
Q5KPD4_CRYNJMICOS complex subunit; Component of the MICOS complex, a large protein complex of the mitochondrial inner membrane that plays crucial roles in the maintenance of crista junctions, inner membrane architecture, and formation of contact sites to the outer membrane. (294 aa)
Q5KQ15_CRYNJConserved expressed protein. (547 aa)
Q5KPE2_CRYNJUncharacterized protein. (159 aa)
Q5KPF8_CRYNJProtein transport protein BOS1; SNARE required for protein transport between the ER and the Golgi complex. (241 aa)
Q5KPI4_CRYNJV-type proton ATPase proteolipid subunit; Proton-conducting pore forming subunit of the membrane integral V0 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. (164 aa)
Q5KPJ0_CRYNJNAD_binding_2 domain-containing protein. (318 aa)
Q5KPL4_CRYNJGLUE N-terminal domain-containing protein. (545 aa)
Q5KPM7_CRYNJChaperone, putative. (103 aa)
Your Current Organism:
Cryptococcus neoformans
NCBI taxonomy Id: 214684
Other names: C. neoformans var. neoformans JEC21, Cryptococcus neoformans JEC21, Cryptococcus neoformans var. neoformans JEC21, Cryptococcus neoformans var. neoformans serotype D JEC21, Cryptococcus neoformans var. neoformans strain JEC21, Filobasidiella neoformans var. neoformans strain JEC21
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