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: 9 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 52 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 70 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4H620
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015877 | biopterin transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015224 | biopterin transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.187 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.212 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.249 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.426 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.616 |
DOC_CDC14_PxL_1 | 623 | 631 | PF14671 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 640 | 646 | PF00134 | 0.379 |
DOC_MAPK_gen_1 | 151 | 157 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 291 | 298 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 511 | 518 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 537 | 545 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 650 | 659 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 291 | 298 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 537 | 545 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.547 |
DOC_PP1_RVXF_1 | 513 | 519 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 640 | 643 | PF13499 | 0.365 |
DOC_PP2B_LxvP_1 | 646 | 649 | PF13499 | 0.331 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.592 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.350 |
LIG_14-3-3_CanoR_1 | 330 | 339 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 515 | 519 | PF00244 | 0.492 |
LIG_APCC_ABBA_1 | 20 | 25 | PF00400 | 0.610 |
LIG_APCC_ABBA_1 | 68 | 73 | PF00400 | 0.643 |
LIG_BRCT_BRCA1_1 | 481 | 485 | PF00533 | 0.318 |
LIG_CSL_BTD_1 | 566 | 569 | PF09270 | 0.399 |
LIG_EVH1_2 | 619 | 623 | PF00568 | 0.361 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.571 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.439 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.357 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.493 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.417 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.592 |
LIG_LIR_Apic_2 | 434 | 440 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 47 | 53 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 142 | 149 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 163 | 173 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 201 | 212 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 484 | 493 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 503 | 509 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 529 | 536 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 584 | 593 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 622 | 631 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 482 | 486 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 529 | 534 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.266 |
LIG_Pex14_1 | 221 | 225 | PF04695 | 0.375 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.287 |
LIG_Pex14_2 | 481 | 485 | PF04695 | 0.312 |
LIG_Pex14_2 | 505 | 509 | PF04695 | 0.373 |
LIG_Rb_pABgroove_1 | 525 | 533 | PF01858 | 0.335 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.513 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.376 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.328 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.516 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.347 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.304 |
LIG_SH2_NCK_1 | 486 | 490 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 587 | 591 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 451 | 454 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.526 |
LIG_SH3_1 | 37 | 43 | PF00018 | 0.626 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.698 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.301 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.597 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.718 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.286 |
LIG_SUMO_SIM_anti_2 | 310 | 319 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 310 | 319 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 569 | 575 | PF11976 | 0.330 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.391 |
LIG_TRFH_1 | 169 | 173 | PF08558 | 0.363 |
LIG_TYR_ITIM | 167 | 172 | PF00017 | 0.382 |
LIG_TYR_ITIM | 284 | 289 | PF00017 | 0.197 |
LIG_TYR_ITSM | 482 | 489 | PF00017 | 0.405 |
LIG_UBA3_1 | 167 | 175 | PF00899 | 0.360 |
LIG_UBA3_1 | 377 | 385 | PF00899 | 0.387 |
LIG_UBA3_1 | 530 | 537 | PF00899 | 0.324 |
LIG_Vh1_VBS_1 | 395 | 413 | PF01044 | 0.409 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.336 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.266 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.558 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.353 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.359 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.563 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.384 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.318 |
MOD_CMANNOS | 221 | 224 | PF00535 | 0.252 |
MOD_Cter_Amidation | 328 | 331 | PF01082 | 0.472 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.725 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.368 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.358 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.373 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.281 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.266 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.673 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.347 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.425 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.581 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.398 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.372 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.376 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.380 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.365 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.375 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.294 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.377 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.602 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.284 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.339 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.346 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.295 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.373 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.299 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.364 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.368 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.356 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.474 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.182 |
MOD_NEK2_2 | 463 | 468 | PF00069 | 0.338 |
MOD_OFUCOSY | 403 | 410 | PF10250 | 0.399 |
MOD_PKA_1 | 330 | 336 | PF00069 | 0.190 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.196 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.351 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.336 |
MOD_Plk_2-3 | 359 | 365 | PF00069 | 0.230 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.346 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.357 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.312 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.395 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.340 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.465 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.320 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.328 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.523 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.383 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.382 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.628 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.593 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.220 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.759 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.419 |
MOD_SUMO_for_1 | 307 | 310 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 655 | 664 | PF00179 | 0.409 |
TRG_DiLeu_BaEn_2 | 45 | 51 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 635 | 640 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.341 |
TRG_NES_CRM1_1 | 459 | 473 | PF08389 | 0.302 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 52% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 55% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 40% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 47% | 99% |
A0A0N1PAY4 | Leptomonas seymouri | 51% | 80% |
A0A0N1PB77 | Leptomonas seymouri | 39% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 61% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 46% | 100% |
A0A381MBI0 | Leishmania infantum | 48% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 48% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 58% | 100% |
A0A3Q8IH50 | Leishmania donovani | 82% | 98% |
A0A3Q8IVN0 | Leishmania donovani | 41% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 47% | 100% |
A0A3S5H5P4 | Leishmania donovani | 50% | 100% |
A0A3S5H5V2 | Leishmania donovani | 47% | 100% |
A0A3S5H6F6 | Leishmania donovani | 57% | 100% |
A0A3S5H763 | Leishmania donovani | 62% | 100% |
A0A3S7WR10 | Leishmania donovani | 51% | 95% |
A0A3S7WR14 | Leishmania donovani | 59% | 100% |
A0A3S7WR15 | Leishmania donovani | 61% | 83% |
A0A3S7WR24 | Leishmania donovani | 58% | 100% |
A4H4T8 | Leishmania braziliensis | 44% | 99% |
A4H5Y4 | Leishmania braziliensis | 48% | 100% |
A4H617 | Leishmania braziliensis | 57% | 100% |
A4H618 | Leishmania braziliensis | 58% | 100% |
A4H619 | Leishmania braziliensis | 58% | 100% |
A4H6C3 | Leishmania braziliensis | 50% | 100% |
A4HNH7 | Leishmania braziliensis | 38% | 100% |
A4HSS2 | Leishmania infantum | 50% | 100% |
A4HUE4 | Leishmania infantum | 50% | 95% |
A4HUE5 | Leishmania infantum | 62% | 100% |
A4HUE6 | Leishmania infantum | 59% | 100% |
A4HUE7 | Leishmania infantum | 58% | 100% |
A4HUE8 | Leishmania infantum | 57% | 100% |
A4HUF4 | Leishmania infantum | 57% | 100% |
A4HUF5 | Leishmania infantum | 82% | 100% |
A4HYA9 | Leishmania infantum | 63% | 100% |
A4IC33 | Leishmania infantum | 40% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AG72 | Leishmania infantum | 47% | 100% |
E9AI40 | Leishmania braziliensis | 62% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 95% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4QDC4 | Leishmania major | 60% | 100% |
Q4QH81 | Leishmania major | 49% | 100% |
Q4QHH7 | Leishmania major | 80% | 100% |
Q4QHH8 | Leishmania major | 55% | 100% |
Q4QHH9 | Leishmania major | 56% | 100% |
Q4QHI0 | Leishmania major | 57% | 99% |
Q4QHI1 | Leishmania major | 61% | 100% |
Q4QHI2 | Leishmania major | 62% | 100% |
Q4QIU9 | Leishmania major | 45% | 100% |
Q4QJ48 | Leishmania major | 50% | 100% |
Q7KIP2 | Leishmania major | 40% | 98% |