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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030008 | TRAPP complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0099023 | vesicle tethering complex | 2 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1990072 | TRAPPIII protein complex | 4 | 1 |
Related structures:
AlphaFold database: E9AK56
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.356 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.294 |
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.614 |
CLV_PCSK_FUR_1 | 83 | 87 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.380 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.686 |
DEG_ODPH_VHL_1 | 516 | 529 | PF01847 | 0.462 |
DEG_SCF_FBW7_1 | 94 | 101 | PF00400 | 0.500 |
DOC_CYCLIN_RxL_1 | 177 | 186 | PF00134 | 0.411 |
DOC_CYCLIN_RxL_1 | 525 | 535 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 39 | 45 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.502 |
DOC_MAPK_HePTP_8 | 289 | 301 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 350 | 358 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 504 | 513 | PF00069 | 0.404 |
DOC_PP1_RVXF_1 | 224 | 231 | PF00149 | 0.302 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.302 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.354 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 39 | 42 | PF13499 | 0.569 |
DOC_PP2B_LxvP_1 | 572 | 575 | PF13499 | 0.500 |
DOC_SPAK_OSR1_1 | 166 | 170 | PF12202 | 0.181 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 184 | 192 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 252 | 262 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 274 | 284 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 377 | 382 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 396 | 401 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 456 | 465 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 566 | 572 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 164 | 181 | PF00022 | 0.356 |
LIG_Actin_WH2_2 | 236 | 251 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 362 | 379 | PF00022 | 0.411 |
LIG_Actin_WH2_2 | 420 | 438 | PF00022 | 0.416 |
LIG_AP2alpha_2 | 79 | 81 | PF02296 | 0.631 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.502 |
LIG_CSL_BTD_1 | 572 | 575 | PF09270 | 0.500 |
LIG_EH1_1 | 366 | 374 | PF00400 | 0.420 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.673 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.365 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.436 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.430 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.555 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.430 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.569 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.454 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.574 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.436 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.532 |
LIG_Integrin_RGD_1 | 599 | 601 | PF01839 | 0.486 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 194 | 204 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.510 |
LIG_NRBOX | 528 | 534 | PF00104 | 0.436 |
LIG_PDZ_Class_2 | 635 | 640 | PF00595 | 0.518 |
LIG_Pex14_1 | 230 | 234 | PF04695 | 0.427 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.406 |
LIG_RPA_C_Fungi | 161 | 173 | PF08784 | 0.261 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.420 |
LIG_SH2_CRK | 522 | 526 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.420 |
LIG_SH2_PTP2 | 250 | 253 | PF00017 | 0.420 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.323 |
LIG_SH3_1 | 477 | 483 | PF00018 | 0.544 |
LIG_SH3_2 | 174 | 179 | PF14604 | 0.411 |
LIG_SH3_2 | 449 | 454 | PF14604 | 0.498 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.744 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.703 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.445 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.410 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.570 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.748 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 542 | 547 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 558 | 564 | PF11976 | 0.499 |
LIG_WW_3 | 451 | 455 | PF00397 | 0.504 |
MOD_CDK_SPK_2 | 391 | 396 | PF00069 | 0.423 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.801 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.427 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.447 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.359 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.532 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.444 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.700 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.754 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.294 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.457 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.599 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.549 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.323 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.763 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.453 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.351 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.473 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.656 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.468 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.684 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.616 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.692 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.249 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.453 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.336 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.379 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.381 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.401 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.448 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.717 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.689 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.410 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.345 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.549 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.677 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.405 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.706 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.335 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.345 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.376 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.470 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.504 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.468 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.422 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.715 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.748 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.734 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.427 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.467 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.574 |
MOD_PKA_1 | 137 | 143 | PF00069 | 0.181 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.181 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.427 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.402 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.471 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.177 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.220 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.287 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.609 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.420 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.473 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.345 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.651 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.420 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.479 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.469 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.404 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.447 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.391 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.725 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.602 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.496 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.763 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 480 | 485 | PF01217 | 0.652 |
TRG_DiLeu_BaLyEn_6 | 525 | 530 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.245 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 553 | 558 | PF00026 | 0.290 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHB8 | Leptomonas seymouri | 48% | 99% |
A0A1X0NLJ7 | Trypanosomatidae | 30% | 100% |
A0A3R7LPQ4 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H5C3 | Leishmania donovani | 86% | 100% |
A4H407 | Leishmania braziliensis | 67% | 99% |
A4HS69 | Leishmania infantum | 86% | 100% |
C9ZY64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
O97215 | Leishmania major | 86% | 100% |
V5BIB6 | Trypanosoma cruzi | 31% | 100% |