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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: E8NHE5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.412 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.655 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.597 |
DOC_ANK_TNKS_1 | 607 | 614 | PF00023 | 0.328 |
DOC_CYCLIN_RxL_1 | 199 | 207 | PF00134 | 0.608 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 288 | 297 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 494 | 500 | PF00134 | 0.340 |
DOC_MAPK_DCC_7 | 455 | 465 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 267 | 273 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.406 |
DOC_PP2B_LxvP_1 | 584 | 587 | PF13499 | 0.499 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.334 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 142 | 146 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 326 | 335 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 345 | 353 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 547 | 554 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 596 | 602 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 71 | 76 | PF00244 | 0.755 |
LIG_Actin_WH2_2 | 409 | 426 | PF00022 | 0.376 |
LIG_APCC_ABBAyCdc20_2 | 401 | 407 | PF00400 | 0.416 |
LIG_BIR_III_4 | 610 | 614 | PF00653 | 0.436 |
LIG_Clathr_ClatBox_1 | 134 | 138 | PF01394 | 0.631 |
LIG_Clathr_ClatBox_1 | 411 | 415 | PF01394 | 0.362 |
LIG_DLG_GKlike_1 | 71 | 78 | PF00625 | 0.592 |
LIG_EH1_1 | 162 | 170 | PF00400 | 0.501 |
LIG_eIF4E_1 | 568 | 574 | PF01652 | 0.320 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.712 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.578 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.538 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.446 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.431 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.487 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.557 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.667 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.564 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 177 | 180 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 324 | 327 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.462 |
LIG_SH3_2 | 587 | 592 | PF14604 | 0.403 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.642 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.377 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.710 |
LIG_SH3_CIN85_PxpxPR_1 | 64 | 69 | PF14604 | 0.605 |
LIG_SUMO_SIM_anti_2 | 176 | 183 | PF11976 | 0.686 |
LIG_SUMO_SIM_anti_2 | 228 | 234 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 479 | 486 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 533 | 539 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 569 | 575 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.683 |
LIG_SUMO_SIM_par_1 | 479 | 486 | PF11976 | 0.332 |
LIG_TYR_ITIM | 566 | 571 | PF00017 | 0.439 |
LIG_UBA3_1 | 164 | 170 | PF00899 | 0.525 |
LIG_UBA3_1 | 252 | 260 | PF00899 | 0.452 |
MOD_CDC14_SPxK_1 | 589 | 592 | PF00782 | 0.388 |
MOD_CDC14_SPxK_1 | 67 | 70 | PF00782 | 0.703 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.704 |
MOD_CDK_SPxK_1 | 586 | 592 | PF00069 | 0.406 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.704 |
MOD_CDK_SPxxK_3 | 64 | 71 | PF00069 | 0.614 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.744 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.675 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.409 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.430 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.570 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.421 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.531 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.292 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.307 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.537 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.303 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.467 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.385 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.499 |
MOD_GlcNHglycan | 415 | 419 | PF01048 | 0.574 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.517 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.480 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.467 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.514 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.723 |
MOD_N-GLC_1 | 504 | 509 | PF02516 | 0.602 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.652 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.711 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.434 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.452 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.664 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.662 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.582 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.497 |
MOD_PKB_1 | 466 | 474 | PF00069 | 0.373 |
MOD_PKB_1 | 69 | 77 | PF00069 | 0.595 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.621 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.635 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.610 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.427 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.312 |
MOD_Plk_2-3 | 262 | 268 | PF00069 | 0.544 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.568 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.628 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.646 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.491 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.348 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.488 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.683 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.383 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.697 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.406 |
TRG_DiLeu_BaEn_1 | 228 | 233 | PF01217 | 0.628 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_1 | 479 | 484 | PF01217 | 0.370 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.671 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.671 |
TRG_NES_CRM1_1 | 251 | 264 | PF08389 | 0.622 |
TRG_NES_CRM1_1 | 421 | 436 | PF08389 | 0.371 |
TRG_NLS_MonoExtN_4 | 66 | 73 | PF00514 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 60% | 96% |
A0A0N1PB02 | Leptomonas seymouri | 39% | 96% |
A0A0S4J6C6 | Bodo saltans | 34% | 98% |
A0A1X0P9A6 | Trypanosomatidae | 37% | 93% |
A0A3Q8IHH1 | Leishmania donovani | 78% | 86% |
A0A3R7K2Y9 | Trypanosoma rangeli | 38% | 92% |
A0A3S5H668 | Leishmania donovani | 35% | 100% |
A0A3S5H669 | Leishmania donovani | 36% | 99% |
A0A3S7X835 | Leishmania donovani | 39% | 100% |
A4H5C9 | Leishmania braziliensis | 35% | 100% |
A4H5D0 | Leishmania braziliensis | 37% | 100% |
A4HAZ7 | Leishmania braziliensis | 39% | 100% |
A4HAZ9 | Leishmania braziliensis | 41% | 100% |
A4HB01 | Leishmania braziliensis | 41% | 100% |
A4HTM0 | Leishmania infantum | 35% | 100% |
A4HTM1 | Leishmania infantum | 35% | 99% |
A4IA57 | Leishmania infantum | 39% | 100% |
C6K3V8 | Leptomonas seymouri | 34% | 100% |
C6K3V9 | Leptomonas seymouri | 33% | 96% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 93% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 99% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4Q1U8 | Leishmania major | 80% | 100% |
Q4Q2R4 | Leishmania major | 38% | 100% |
Q4Q310 | Leishmania major | 77% | 100% |
Q4Q312 | Leishmania major | 77% | 100% |
Q4Q340 | Leishmania major | 77% | 100% |
Q4Q342 | Leishmania major | 77% | 100% |
Q4QI90 | Leishmania major | 35% | 100% |
Q4QI91 | Leishmania major | 35% | 100% |