Intracellular protein trafficking, EAP30/Vps36 family, putative
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000814 | ESCRT II complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0036452 | ESCRT complex | 2 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I9V9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0071985 | multivesicular body sorting pathway | 5 | 12 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0007034 | vacuolar transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 1 |
GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0043328 | protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0045324 | late endosome to vacuole transport | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072665 | protein localization to vacuole | 6 | 1 |
GO:0072666 | establishment of protein localization to vacuole | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.448 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.714 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.615 |
CLV_PCSK_PC7_1 | 315 | 321 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.273 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.539 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.522 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.448 |
DOC_PP1_RVXF_1 | 120 | 126 | PF00149 | 0.539 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 364 | 368 | PF12436 | 0.618 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 239 | 243 | PF00244 | 0.490 |
LIG_APCC_ABBAyCdc20_2 | 82 | 88 | PF00400 | 0.491 |
LIG_BIR_III_4 | 88 | 92 | PF00653 | 0.491 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.457 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.491 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.405 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.515 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.651 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.448 |
LIG_GBD_Chelix_1 | 70 | 78 | PF00786 | 0.304 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.439 |
LIG_PALB2_WD40_1 | 382 | 390 | PF16756 | 0.488 |
LIG_REV1ctd_RIR_1 | 123 | 133 | PF16727 | 0.539 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 117 | 120 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.504 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 211 | 217 | PF11976 | 0.506 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.572 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.701 |
LIG_TYR_ITIM | 383 | 388 | PF00017 | 0.529 |
LIG_UBA3_1 | 175 | 181 | PF00899 | 0.539 |
MOD_CDC14_SPxK_1 | 349 | 352 | PF00782 | 0.642 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.650 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.530 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.518 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.453 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.491 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.689 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.270 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.324 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.285 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.313 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.355 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.391 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.614 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.498 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.471 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.568 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.527 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.502 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.491 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.609 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.654 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.278 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.414 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.587 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.454 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.466 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.496 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.433 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.697 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.705 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.447 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.476 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.493 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.769 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.545 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.475 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.582 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.529 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.488 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.422 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.448 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 105 | 113 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 163 | 168 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 358 | 366 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 376 | 383 | PF00179 | 0.384 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.293 |
TRG_PTS2 | 1 | 39 | PF00400 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSW5 | Leptomonas seymouri | 71% | 100% |
A0A0S4J518 | Bodo saltans | 27% | 96% |
A0A1X0P9K2 | Trypanosomatidae | 45% | 100% |
A0A3Q8IKY6 | Leishmania donovani | 100% | 100% |
A0A3R7NWX2 | Trypanosoma rangeli | 44% | 100% |
A4H7S7 | Leishmania braziliensis | 78% | 100% |
C9ZMT0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B4X2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q355 | Leishmania major | 92% | 100% |
V5BT20 | Trypanosoma cruzi | 42% | 100% |