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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H3T1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.856 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 579 | 583 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 581 | 583 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.503 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.424 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.340 |
DEG_SPOP_SBC_1 | 585 | 589 | PF00917 | 0.674 |
DOC_CYCLIN_RxL_1 | 392 | 402 | PF00134 | 0.509 |
DOC_MAPK_gen_1 | 17 | 26 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 341 | 350 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.472 |
DOC_MAPK_NFAT4_5 | 122 | 130 | PF00069 | 0.394 |
DOC_PP1_RVXF_1 | 344 | 350 | PF00149 | 0.266 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.833 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.866 |
DOC_USP7_MATH_2 | 533 | 539 | PF00917 | 0.859 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.696 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.463 |
LIG_EVH1_2 | 70 | 74 | PF00568 | 0.515 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.387 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.312 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.494 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.435 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.385 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.701 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.785 |
LIG_GBD_Chelix_1 | 347 | 355 | PF00786 | 0.261 |
LIG_IRF3_LxIS_1 | 486 | 493 | PF10401 | 0.650 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 374 | 384 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.365 |
LIG_MYND_1 | 71 | 75 | PF01753 | 0.622 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.536 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 423 | 427 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 465 | 468 | PF00017 | 0.800 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.659 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.299 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.741 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.555 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.807 |
LIG_SUMO_SIM_anti_2 | 226 | 234 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 356 | 361 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 497 | 502 | PF11976 | 0.652 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.627 |
LIG_WW_3 | 69 | 73 | PF00397 | 0.523 |
MOD_CDK_SPK_2 | 501 | 506 | PF00069 | 0.841 |
MOD_CDK_SPxK_1 | 539 | 545 | PF00069 | 0.865 |
MOD_CDK_SPxxK_3 | 539 | 546 | PF00069 | 0.865 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.482 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.304 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.516 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.467 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.537 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.801 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.693 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.757 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.418 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.469 |
MOD_CMANNOS | 18 | 21 | PF00535 | 0.358 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.648 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.614 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.608 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.477 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.454 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.315 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.462 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.468 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.501 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.650 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.778 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.864 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.789 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.771 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.241 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.450 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.485 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.409 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.515 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.440 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.456 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.499 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.411 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.510 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.418 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.731 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.806 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.659 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.342 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.529 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.474 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.673 |
MOD_PKA_1 | 581 | 587 | PF00069 | 0.706 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.516 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.503 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.694 |
MOD_PKB_1 | 547 | 555 | PF00069 | 0.782 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.485 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.452 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.314 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.524 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.626 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.664 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.770 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.683 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.798 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.480 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.799 |
TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 432 | 437 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 479 | 484 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X8 | Leptomonas seymouri | 50% | 96% |
A0A451EJV6 | Leishmania donovani | 77% | 100% |
A4HS06 | Leishmania infantum | 77% | 100% |
E9AJZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q9N858 | Leishmania major | 78% | 97% |