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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 5, no: 6 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0005793 | endoplasmic reticulum-Golgi intermediate compartment | 5 | 1 |
GO:0030134 | COPII-coated ER to Golgi transport vesicle | 8 | 1 |
GO:0030135 | coated vesicle | 7 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AKL4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007029 | endoplasmic reticulum organization | 5 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005537 | mannose binding | 4 | 1 |
GO:0030246 | carbohydrate binding | 2 | 2 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0048029 | monosaccharide binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 446 | 450 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.682 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.647 |
CLV_PCSK_PC7_1 | 235 | 241 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 323 | 329 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.638 |
CLV_Separin_Metazoa | 408 | 412 | PF03568 | 0.392 |
DEG_APCC_DBOX_1 | 447 | 455 | PF00400 | 0.526 |
DEG_APCC_DBOX_1 | 472 | 480 | PF00400 | 0.297 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.577 |
DOC_CYCLIN_RxL_1 | 229 | 242 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 373 | 383 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 503 | 509 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 376 | 383 | PF00069 | 0.292 |
DOC_PP1_RVXF_1 | 504 | 510 | PF00149 | 0.430 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.350 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.244 |
DOC_SPAK_OSR1_1 | 123 | 127 | PF12202 | 0.244 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.398 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 240 | 245 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 449 | 455 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.257 |
LIG_deltaCOP1_diTrp_1 | 116 | 124 | PF00928 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 183 | 191 | PF00928 | 0.476 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.275 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.392 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.340 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.426 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.492 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.275 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.532 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.427 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.347 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.384 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.377 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.548 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 62 | 68 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.269 |
LIG_PDZ_Class_3 | 517 | 522 | PF00595 | 0.497 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.488 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.340 |
LIG_PTB_Apo_2 | 87 | 94 | PF02174 | 0.257 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 413 | 417 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 152 | 155 | PF00017 | 0.257 |
LIG_SH2_STAT3 | 374 | 377 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.349 |
LIG_SH3_1 | 511 | 517 | PF00018 | 0.436 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.485 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.438 |
LIG_SUMO_SIM_anti_2 | 365 | 372 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 404 | 412 | PF11976 | 0.398 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.464 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.376 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.400 |
LIG_UBA3_1 | 233 | 239 | PF00899 | 0.623 |
MOD_CDK_SPxxK_3 | 169 | 176 | PF00069 | 0.645 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.559 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.399 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.512 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.515 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.657 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.503 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.492 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.479 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.452 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.412 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.643 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.363 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.300 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.641 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.514 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.579 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.590 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.475 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.417 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.395 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.548 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.369 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.411 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.343 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.486 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.631 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.425 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.195 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.581 |
MOD_PK_1 | 240 | 246 | PF00069 | 0.561 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.645 |
MOD_PKA_1 | 239 | 245 | PF00069 | 0.471 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.239 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.279 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.627 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.621 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.432 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.483 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.298 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.523 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.298 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.666 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.454 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.350 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.463 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.534 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.359 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.464 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.646 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.387 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.492 |
MOD_SUMO_for_1 | 389 | 392 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 453 | 463 | PF00179 | 0.555 |
MOD_SUMO_rev_2 | 478 | 486 | PF00179 | 0.404 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.625 |
TRG_NES_CRM1_1 | 470 | 482 | PF08389 | 0.552 |
TRG_NLS_MonoCore_2 | 225 | 230 | PF00514 | 0.611 |
TRG_NLS_MonoCore_2 | 445 | 450 | PF00514 | 0.572 |
TRG_NLS_MonoExtC_3 | 225 | 230 | PF00514 | 0.611 |
TRG_NLS_MonoExtC_3 | 445 | 450 | PF00514 | 0.572 |
TRG_NLS_MonoExtN_4 | 223 | 230 | PF00514 | 0.621 |
TRG_NLS_MonoExtN_4 | 444 | 451 | PF00514 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA0 | Leptomonas seymouri | 77% | 100% |
A0A1X0NKB0 | Trypanosomatidae | 43% | 81% |
A0A3R7LT82 | Trypanosoma rangeli | 47% | 96% |
A0A3S5H5L7 | Leishmania donovani | 92% | 86% |
A4H4F2 | Leishmania braziliensis | 88% | 100% |
A4HSM9 | Leishmania infantum | 93% | 100% |
C9ZU67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 84% |
E8NHN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
Q4QJ95 | Leishmania major | 94% | 100% |
V5ARI9 | Trypanosoma cruzi | 46% | 89% |