N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. Localization: Golgi (by homology)
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. | yes | yes: 125 |
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: 32 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 39 |
NetGPI | no | yes: 0, no: 39 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0016020 | membrane | 2 | 19 |
Related structures:
AlphaFold database: Q4QES0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 38 |
GO:0016740 | transferase activity | 2 | 38 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.378 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 801 | 805 | PF00656 | 0.394 |
CLV_MEL_PAP_1 | 92 | 98 | PF00089 | 0.493 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.601 |
CLV_PCSK_FUR_1 | 410 | 414 | PF00082 | 0.555 |
CLV_PCSK_FUR_1 | 483 | 487 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.520 |
DEG_APCC_DBOX_1 | 194 | 202 | PF00400 | 0.437 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.532 |
DOC_CDC14_PxL_1 | 121 | 129 | PF14671 | 0.370 |
DOC_CKS1_1 | 570 | 575 | PF01111 | 0.626 |
DOC_CYCLIN_yCln2_LP_2 | 453 | 459 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 791 | 797 | PF00134 | 0.408 |
DOC_MAPK_DCC_7 | 538 | 547 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 206 | 215 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 280 | 289 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 446 | 457 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 538 | 547 | PF00069 | 0.545 |
DOC_MAPK_HePTP_8 | 566 | 578 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 448 | 457 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 569 | 578 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 634 | 641 | PF00069 | 0.624 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 740 | 743 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 570 | 573 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 364 | 371 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 486 | 495 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 638 | 642 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 659 | 667 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 808 | 812 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.633 |
LIG_Actin_WH2_2 | 236 | 253 | PF00022 | 0.459 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 596 | 600 | PF00533 | 0.624 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.465 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.315 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.605 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.473 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.478 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.586 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.426 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.525 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.444 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.582 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.474 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.539 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.527 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.464 |
LIG_LIR_Apic_2 | 120 | 125 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 792 | 796 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 806 | 812 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 100 | 111 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 519 | 529 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 798 | 807 | PF02991 | 0.572 |
LIG_LIR_LC3C_4 | 763 | 768 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.518 |
LIG_MAD2 | 659 | 667 | PF02301 | 0.528 |
LIG_MYND_1 | 74 | 78 | PF01753 | 0.554 |
LIG_PTB_Apo_2 | 129 | 136 | PF02174 | 0.549 |
LIG_PTB_Apo_2 | 289 | 296 | PF02174 | 0.361 |
LIG_PTB_Apo_2 | 540 | 547 | PF02174 | 0.478 |
LIG_PTB_Phospho_1 | 129 | 135 | PF10480 | 0.401 |
LIG_PTB_Phospho_1 | 289 | 295 | PF10480 | 0.361 |
LIG_PTB_Phospho_1 | 540 | 546 | PF10480 | 0.511 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.487 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.437 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 165 | 168 | PF00017 | 0.414 |
LIG_SH2_GRB2like | 290 | 293 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 546 | 549 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.443 |
LIG_SH2_SRC | 395 | 398 | PF00017 | 0.436 |
LIG_SH2_SRC | 575 | 578 | PF00017 | 0.545 |
LIG_SH2_SRC | 614 | 617 | PF00017 | 0.555 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.223 |
LIG_SH2_STAT3 | 671 | 674 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.558 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.460 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.575 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.512 |
LIG_SH3_CIN85_PxpxPR_1 | 404 | 409 | PF14604 | 0.515 |
LIG_SUMO_SIM_anti_2 | 38 | 45 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 763 | 769 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 211 | 216 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 383 | 389 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 745 | 751 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 763 | 769 | PF11976 | 0.363 |
LIG_TRAF2_1 | 590 | 593 | PF00917 | 0.553 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.544 |
LIG_TYR_ITIM | 101 | 106 | PF00017 | 0.552 |
LIG_TYR_ITIM | 438 | 443 | PF00017 | 0.354 |
LIG_WRC_WIRS_1 | 102 | 107 | PF05994 | 0.477 |
MOD_CDK_SPK_2 | 468 | 473 | PF00069 | 0.449 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.608 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.397 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.427 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.475 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.524 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.433 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.524 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.575 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.495 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.563 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.463 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.577 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.565 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.577 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.497 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.604 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.640 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.515 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.605 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.509 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.653 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.488 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.599 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.479 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.608 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.387 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.527 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.675 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.597 |
MOD_LATS_1 | 249 | 255 | PF00433 | 0.359 |
MOD_LATS_1 | 411 | 417 | PF00433 | 0.406 |
MOD_LATS_1 | 444 | 450 | PF00433 | 0.275 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.523 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.552 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.561 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.456 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.526 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.344 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.413 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.388 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.413 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.562 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.421 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.481 |
MOD_NEK2_2 | 439 | 444 | PF00069 | 0.298 |
MOD_NEK2_2 | 645 | 650 | PF00069 | 0.518 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.549 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.485 |
MOD_PK_1 | 446 | 452 | PF00069 | 0.255 |
MOD_PK_1 | 682 | 688 | PF00069 | 0.687 |
MOD_PKA_1 | 446 | 452 | PF00069 | 0.265 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.418 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.433 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.383 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.337 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.355 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.399 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.326 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.548 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.617 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.556 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.637 |
MOD_PKB_1 | 280 | 288 | PF00069 | 0.380 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.475 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.380 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.457 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.427 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.535 |
MOD_Plk_2-3 | 673 | 679 | PF00069 | 0.633 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.472 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.481 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.484 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.417 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.381 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.596 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.450 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.358 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.391 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.499 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.671 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.625 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.576 |
MOD_TYR_CSK | 60 | 68 | PF07714 | 0.521 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_1 | 786 | 791 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 72 | 78 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 800 | 803 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 714 | 717 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Q7 | Leptomonas seymouri | 46% | 100% |
A0A1X0NYY7 | Trypanosomatidae | 43% | 100% |
A0A3Q8IAD3 | Leishmania donovani | 54% | 83% |
A0A3Q8IAF8 | Leishmania donovani | 72% | 84% |
A0A3Q8IAK8 | Leishmania donovani | 78% | 83% |
A0A3Q8IJ32 | Leishmania donovani | 89% | 98% |
A0A3S5H6Y1 | Leishmania donovani | 76% | 86% |
A0A3S7WTZ8 | Leishmania donovani | 62% | 79% |
A0A3S7WU13 | Leishmania donovani | 90% | 86% |
A0A422NAR5 | Trypanosoma rangeli | 44% | 100% |
A4H8M5 | Leishmania braziliensis | 70% | 90% |
A4H8M6 | Leishmania braziliensis | 83% | 100% |
A4H8M7 | Leishmania braziliensis | 81% | 88% |
A4H8N0 | Leishmania braziliensis | 50% | 100% |
A4H8N1 | Leishmania braziliensis | 53% | 83% |
A4HWZ5 | Leishmania infantum | 91% | 86% |
A4HWZ6 | Leishmania infantum | 73% | 89% |
A4HWZ8 | Leishmania infantum | 76% | 89% |
A4HX00 | Leishmania infantum | 62% | 79% |
A4HX01 | Leishmania infantum | 54% | 100% |
A4HX05 | Leishmania infantum | 71% | 84% |
E8NHI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 87% |
E9AGP0 | Leishmania infantum | 81% | 100% |
E9AQQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 94% |
E9AQR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 82% |
E9AQR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 87% |
E9AQR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 85% |
E9AQR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 80% |
E9AQR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 83% |
Q4QER2 | Leishmania major | 55% | 100% |
Q4QER3 | Leishmania major | 65% | 100% |
Q4QER4 | Leishmania major | 84% | 100% |
Q4QER5 | Leishmania major | 96% | 100% |
Q4QER6 | Leishmania major | 96% | 100% |
Q4QER7 | Leishmania major | 89% | 100% |
Q4QER8 | Leishmania major | 80% | 100% |
Q4QER9 | Leishmania major | 79% | 100% |
V5ANJ8 | Trypanosoma cruzi | 44% | 100% |