STRINGSTRING
T1FXT6_HELRO T1FXT6_HELRO T1FXW6_HELRO T1FXW6_HELRO T1FYF9_HELRO T1FYF9_HELRO T1FZ29_HELRO T1FZ29_HELRO T1FZ41_HELRO T1FZ41_HELRO T1FZA0_HELRO T1FZA0_HELRO T1FZC8_HELRO T1FZC8_HELRO T1FZI5_HELRO T1FZI5_HELRO T1FZU1_HELRO T1FZU1_HELRO T1FZY6_HELRO T1FZY6_HELRO T1G006_HELRO T1G006_HELRO T1G0C3_HELRO T1G0C3_HELRO T1G0E3_HELRO T1G0E3_HELRO T1G1E7_HELRO T1G1E7_HELRO T1G1I5_HELRO T1G1I5_HELRO T1G1K3_HELRO T1G1K3_HELRO T1G287_HELRO T1G287_HELRO T1G2C5_HELRO T1G2C5_HELRO T1G2E5_HELRO T1G2E5_HELRO T1G2F8_HELRO T1G2F8_HELRO T1G2T0_HELRO T1G2T0_HELRO T1G344_HELRO T1G344_HELRO T1G388_HELRO T1G388_HELRO T1G3H2_HELRO T1G3H2_HELRO T1G4Y9_HELRO T1G4Y9_HELRO T1G522_HELRO T1G522_HELRO T1G5I0_HELRO T1G5I0_HELRO T1G644_HELRO T1G644_HELRO T1G687_HELRO T1G687_HELRO T1G6D3_HELRO T1G6D3_HELRO T1G6J2_HELRO T1G6J2_HELRO T1G747_HELRO T1G747_HELRO T1G7X1_HELRO T1G7X1_HELRO T1G8B3_HELRO T1G8B3_HELRO T1G8F2_HELRO T1G8F2_HELRO T1G8V0_HELRO T1G8V0_HELRO T1G933_HELRO T1G933_HELRO T1G9D6_HELRO T1G9D6_HELRO T1ED49_HELRO T1ED49_HELRO T1ED33_HELRO T1ED33_HELRO T1ED20_HELRO T1ED20_HELRO T1EFQ6_HELRO T1EFQ6_HELRO T1ED88_HELRO T1ED88_HELRO T1ED97_HELRO T1ED97_HELRO T1EDD4_HELRO T1EDD4_HELRO T1EDI0_HELRO T1EDI0_HELRO T1EE90_HELRO T1EE90_HELRO T1EEI6_HELRO T1EEI6_HELRO T1EEP9_HELRO T1EEP9_HELRO T1EEV1_HELRO T1EEV1_HELRO T1EEW2_HELRO T1EEW2_HELRO T1EF73_HELRO T1EF73_HELRO T1EFD4_HELRO T1EFD4_HELRO T1EE97_HELRO T1EE97_HELRO T1EEE1_HELRO T1EEE1_HELRO T1EFQ0_HELRO T1EFQ0_HELRO T1EGL1_HELRO T1EGL1_HELRO T1EG28_HELRO T1EG28_HELRO T1EG03_HELRO T1EG03_HELRO T1EFS4_HELRO T1EFS4_HELRO T1EI01_HELRO T1EI01_HELRO T1EIK8_HELRO T1EIK8_HELRO T1EJC8_HELRO T1EJC8_HELRO T1EKQ4_HELRO T1EKQ4_HELRO T1ELN6_HELRO T1ELN6_HELRO T1ELQ1_HELRO T1ELQ1_HELRO T1ELU7_HELRO T1ELU7_HELRO T1EM38_HELRO T1EM38_HELRO T1EM62_HELRO T1EM62_HELRO T1EMB3_HELRO T1EMB3_HELRO T1EMC9_HELRO T1EMC9_HELRO T1EMF2_HELRO T1EMF2_HELRO T1EMT4_HELRO T1EMT4_HELRO T1ENQ3_HELRO T1ENQ3_HELRO T1ERD1_HELRO T1ERD1_HELRO T1ESC4_HELRO T1ESC4_HELRO T1EUB7_HELRO T1EUB7_HELRO T1EVS7_HELRO T1EVS7_HELRO T1EX14_HELRO T1EX14_HELRO T1F0C0_HELRO T1F0C0_HELRO T1F0E8_HELRO T1F0E8_HELRO T1F186_HELRO T1F186_HELRO T1F187_HELRO T1F187_HELRO T1F3D7_HELRO T1F3D7_HELRO T1F3T0_HELRO T1F3T0_HELRO T1F4Z3_HELRO T1F4Z3_HELRO T1F5B0_HELRO T1F5B0_HELRO T1F763_HELRO T1F763_HELRO T1F892_HELRO T1F892_HELRO T1F8K5_HELRO T1F8K5_HELRO T1FAP4_HELRO T1FAP4_HELRO T1FAP5_HELRO T1FAP5_HELRO T1FAR0_HELRO T1FAR0_HELRO T1FCF8_HELRO T1FCF8_HELRO T1FH98_HELRO T1FH98_HELRO T1FHE9_HELRO T1FHE9_HELRO T1FKL6_HELRO T1FKL6_HELRO T1FL31_HELRO T1FL31_HELRO T1FM72_HELRO T1FM72_HELRO T1FME0_HELRO T1FME0_HELRO T1FMG8_HELRO T1FMG8_HELRO T1FMZ1_HELRO T1FMZ1_HELRO T1FN28_HELRO T1FN28_HELRO T1FNA1_HELRO T1FNA1_HELRO T1FNE3_HELRO T1FNE3_HELRO T1FNG8_HELRO T1FNG8_HELRO T1FNM9_HELRO T1FNM9_HELRO T1FNQ3_HELRO T1FNQ3_HELRO T1FP19_HELRO T1FP19_HELRO T1FP49_HELRO T1FP49_HELRO T1FP91_HELRO T1FP91_HELRO T1FPJ3_HELRO T1FPJ3_HELRO T1FPR6_HELRO T1FPR6_HELRO T1FPV2_HELRO T1FPV2_HELRO T1FQ69_HELRO T1FQ69_HELRO T1FR09_HELRO T1FR09_HELRO T1FR43_HELRO T1FR43_HELRO T1FSQ8_HELRO T1FSQ8_HELRO T1FSS6_HELRO T1FSS6_HELRO T1FTL0_HELRO T1FTL0_HELRO T1FTP8_HELRO T1FTP8_HELRO T1FU32_HELRO T1FU32_HELRO T1FUC5_HELRO T1FUC5_HELRO T1FUU5_HELRO T1FUU5_HELRO T1FVW4_HELRO T1FVW4_HELRO T1FVX9_HELRO T1FVX9_HELRO T1FW21_HELRO T1FW21_HELRO T1FWD1_HELRO T1FWD1_HELRO T1FWF2_HELRO T1FWF2_HELRO T1FWP7_HELRO T1FWP7_HELRO T1FWQ7_HELRO T1FWQ7_HELRO T1FWZ3_HELRO T1FWZ3_HELRO T1FXK8_HELRO T1FXK8_HELRO T1FXQ0_HELRO T1FXQ0_HELRO
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.
Node Color
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
Others
textmining
co-expression
protein homology
Your Input:
T1FXT6_HELROArf-GAP domain-containing protein. (137 aa)
T1FXW6_HELROCoatomer 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. (171 aa)
T1FYF9_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (381 aa)
T1FZ29_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (187 aa)
T1FZ41_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (189 aa)
T1FZA0_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (386 aa)
T1FZC8_HELRODynein light chain. (89 aa)
T1FZI5_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (685 aa)
T1FZU1_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (635 aa)
T1FZY6_HELROPH domain-containing protein. (613 aa)
T1G006_HELROGOLD domain-containing protein. (210 aa)
T1G0C3_HELROGOLD domain-containing protein. (215 aa)
T1G0E3_HELROUncharacterized protein. (855 aa)
T1G1E7_HELROGuanine nucleotide-binding protein subunit gamma; Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction. (70 aa)
T1G1I5_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (82 aa)
T1G1K3_HELROGpcrRhopsn4 domain-containing protein. (327 aa)
T1G287_HELROGOLD domain-containing protein. (217 aa)
T1G2C5_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (387 aa)
T1G2E5_HELROUncharacterized protein. (376 aa)
T1G2F8_HELROUncharacterized protein. (217 aa)
T1G2T0_HELROUncharacterized protein. (755 aa)
T1G344_HELROSEC7 domain-containing protein. (1771 aa)
T1G388_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (326 aa)
T1G3H2_HELROUncharacterized protein. (184 aa)
T1G4Y9_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (368 aa)
T1G522_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (178 aa)
T1G5I0_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (451 aa)
T1G644_HELROUncharacterized protein. (269 aa)
T1G687_HELROGuanine nucleotide-binding protein subunit gamma; Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction. (66 aa)
T1G6D3_HELROF-actin-capping protein subunit beta; F-actin-capping proteins bind in a Ca(2+)-independent manner to the fast growing ends of actin filaments (barbed end) thereby blocking the exchange of subunits at these ends. Unlike other capping proteins (such as gelsolin and severin), these proteins do not sever actin filaments. (276 aa)
T1G6J2_HELROLissencephaly-1 homolog; Positively regulates the activity of the minus-end directed microtubule motor protein dynein. May enhance dynein-mediated microtubule sliding by targeting dynein to the microtubule plus end. Required for several dynein- and microtubule-dependent processes. (410 aa)
T1G747_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (561 aa)
T1G7X1_HELROUncharacterized protein; Belongs to the synaptobrevin family. (214 aa)
T1G8B3_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (519 aa)
T1G8F2_HELROPNPLA domain-containing protein. (330 aa)
T1G8V0_HELROTubulin beta chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (445 aa)
T1G933_HELROTubulin alpha chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (450 aa)
T1G9D6_HELROCoatomer 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. (1004 aa)
T1ED49_HELROCoatomer 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. (1228 aa)
T1ED33_HELROCoatomer 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. (958 aa)
T1ED20_HELROGpcrRhopsn4 domain-containing protein. (504 aa)
T1EFQ6_HELROCoatomer 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. (177 aa)
T1ED88_HELRODynactin domain-containing protein. (587 aa)
T1ED97_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (327 aa)
T1EDD4_HELROCoatomer 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. (303 aa)
T1EDI0_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (677 aa)
T1EE90_HELROArf-GAP domain-containing protein. (435 aa)
T1EEI6_HELROUncharacterized protein. (51 aa)
T1EEP9_HELROUncharacterized protein. (1123 aa)
T1EEV1_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (1237 aa)
T1EEW2_HELROGOLD domain-containing protein. (217 aa)
T1EF73_HELROUncharacterized protein. (270 aa)
T1EFD4_HELROSyntaxin-18_N domain-containing protein. (337 aa)
T1EE97_HELROF-actin-capping protein subunit alpha; F-actin-capping proteins bind in a Ca(2+)-independent manner to the fast growing ends of actin filaments (barbed end) thereby blocking the exchange of subunits at these ends. Unlike other capping proteins (such as gelsolin and severin), these proteins do not sever actin filaments. (291 aa)
T1EEE1_HELROUncharacterized protein. (426 aa)
T1EFQ0_HELROUncharacterized protein. (292 aa)
T1EGL1_HELROPNPLA domain-containing protein. (331 aa)
T1EG28_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (587 aa)
T1EG03_HELROTPR_REGION domain-containing protein. (553 aa)
T1EFS4_HELROTPR_REGION domain-containing protein. (614 aa)
T1EI01_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (290 aa)
T1EIK8_HELROCAP-Gly domain-containing protein. (74 aa)
T1EJC8_HELROGOLD domain-containing protein. (200 aa)
T1EKQ4_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (127 aa)
T1ELN6_HELROCoatomer 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. (856 aa)
T1ELQ1_HELROTubulin beta chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (451 aa)
T1ELU7_HELROUncharacterized protein. (202 aa)
T1EM38_HELROUncharacterized protein. (270 aa)
T1EM62_HELROER lumen protein-retaining receptor. (212 aa)
T1EMB3_HELROUncharacterized protein. (292 aa)
T1EMC9_HELROUncharacterized protein. (152 aa)
T1EMF2_HELROUncharacterized protein. (181 aa)
T1EMT4_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (622 aa)
T1ENQ3_HELROTPR_REGION domain-containing protein. (751 aa)
T1ERD1_HELROUncharacterized protein. (203 aa)
T1ESC4_HELROUncharacterized protein. (238 aa)
T1EUB7_HELROSGNH_hydro domain-containing protein. (231 aa)
T1EVS7_HELROUncharacterized protein. (712 aa)
T1EX14_HELROUncharacterized protein. (2000 aa)
T1F0C0_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (608 aa)
T1F0E8_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (167 aa)
T1F186_HELROUncharacterized protein. (531 aa)
T1F187_HELROUncharacterized protein. (147 aa)
T1F3D7_HELROUncharacterized protein. (282 aa)
T1F3T0_HELROUncharacterized protein. (800 aa)
T1F4Z3_HELROUncharacterized protein. (461 aa)
T1F5B0_HELROUncharacterized protein. (592 aa)
T1F763_HELROER lumen protein-retaining receptor. (212 aa)
T1F892_HELROUncharacterized protein. (1472 aa)
T1F8K5_HELRONbas_N domain-containing protein. (712 aa)
T1FAP4_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (371 aa)
T1FAP5_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (188 aa)
T1FAR0_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (1242 aa)
T1FCF8_HELRORho-GAP domain-containing protein. (447 aa)
T1FH98_HELROKinesin-like protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (629 aa)
T1FHE9_HELROTubulin beta chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (489 aa)
T1FKL6_HELROANK_REP_REGION domain-containing protein. (158 aa)
T1FL31_HELROUncharacterized protein. (364 aa)
T1FM72_HELROUncharacterized protein. (312 aa)
T1FME0_HELROUncharacterized protein. (242 aa)
T1FMG8_HELROTubulin alpha chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (450 aa)
T1FMZ1_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (180 aa)
T1FN28_HELRODynein light intermediate chain; Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function. Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. May play a role in binding dynein to membranous organelles or chromosomes. (462 aa)
T1FNA1_HELROUncharacterized protein. (205 aa)
T1FNE3_HELROTubulin alpha chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (451 aa)
T1FNG8_HELROUncharacterized protein. (204 aa)
T1FNM9_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (181 aa)
T1FNQ3_HELROTubulin beta chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (449 aa)
T1FP19_HELROUncharacterized protein; Belongs to the tubulin family. (441 aa)
T1FP49_HELROTubulin beta chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (449 aa)
T1FP91_HELROUncharacterized protein; Belongs to the actin family. (418 aa)
T1FPJ3_HELROUncharacterized protein. (2070 aa)
T1FPR6_HELROUncharacterized protein. (363 aa)
T1FPV2_HELROUncharacterized protein. (3276 aa)
T1FQ69_HELROCoatomer 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. (512 aa)
T1FR09_HELROUncharacterized protein. (440 aa)
T1FR43_HELROUncharacterized protein. (738 aa)
T1FSQ8_HELROUncharacterized protein. (894 aa)
T1FSS6_HELRODynein light intermediate chain; Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function. Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. May play a role in binding dynein to membranous organelles or chromosomes. (448 aa)
T1FTL0_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (1133 aa)
T1FTP8_HELROUncharacterized protein. (357 aa)
T1FU32_HELROUncharacterized protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (1366 aa)
T1FUC5_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (717 aa)
T1FUU5_HELROUncharacterized protein. (483 aa)
T1FVW4_HELROUncharacterized protein. (209 aa)
T1FVX9_HELROUncharacterized protein. (783 aa)
T1FW21_HELROTubulin alpha chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (459 aa)
T1FWD1_HELROKinesin motor domain-containing protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. (1007 aa)
T1FWF2_HELROUncharacterized protein. (303 aa)
T1FWP7_HELROUncharacterized protein. (787 aa)
T1FWQ7_HELROUncharacterized protein. (459 aa)
T1FWZ3_HELROUncharacterized protein. (273 aa)
T1FXK8_HELROER lumen protein-retaining receptor. (213 aa)
T1FXQ0_HELROUncharacterized protein; Belongs to the small GTPase superfamily. Arf family. (176 aa)
Your Current Organism:
Helobdella robusta
NCBI taxonomy Id: 6412
Other names: H. robusta
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