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 |
Related structures:
AlphaFold database: E9B2L7
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 1 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 684 | 688 | PF00656 | 0.550 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 673 | 675 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.397 |
CLV_Separin_Metazoa | 61 | 65 | PF03568 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.356 |
DEG_ODPH_VHL_1 | 294 | 305 | PF01847 | 0.465 |
DEG_ODPH_VHL_1 | 444 | 457 | PF01847 | 0.609 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.562 |
DEG_SPOP_SBC_1 | 638 | 642 | PF00917 | 0.619 |
DEG_SPOP_SBC_1 | 662 | 666 | PF00917 | 0.422 |
DOC_CDC14_PxL_1 | 100 | 108 | PF14671 | 0.651 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.557 |
DOC_CKS1_1 | 474 | 479 | PF01111 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 253 | 259 | PF00134 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 392 | 398 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 474 | 480 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 266 | 272 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 327 | 336 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 370 | 379 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 95 | 102 | PF00069 | 0.623 |
DOC_MAPK_HePTP_8 | 367 | 379 | PF00069 | 0.543 |
DOC_MAPK_HePTP_8 | 386 | 398 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 108 | 115 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 370 | 379 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 389 | 398 | PF00069 | 0.413 |
DOC_MAPK_NFAT4_5 | 389 | 397 | PF00069 | 0.508 |
DOC_MAPK_RevD_3 | 251 | 267 | PF00069 | 0.526 |
DOC_MIT_MIM_1 | 297 | 306 | PF04212 | 0.577 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.503 |
DOC_PP1_RVXF_1 | 449 | 456 | PF00149 | 0.569 |
DOC_PP1_RVXF_1 | 96 | 103 | PF00149 | 0.626 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.575 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.594 |
DOC_PP2B_LxvP_1 | 392 | 395 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.573 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 595 | 599 | PF12436 | 0.658 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.585 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 214 | 224 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 512 | 522 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 682 | 687 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.627 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 561 | 565 | PF00533 | 0.586 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.578 |
LIG_DLG_GKlike_1 | 682 | 690 | PF00625 | 0.516 |
LIG_EH1_1 | 480 | 488 | PF00400 | 0.544 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.578 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.636 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.616 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.570 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.520 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.653 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.516 |
LIG_FHA_1 | 633 | 639 | PF00498 | 0.575 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.652 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.606 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.708 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.553 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.528 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 603 | 607 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 307 | 317 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 562 | 570 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 665 | 675 | PF02991 | 0.622 |
LIG_LIR_LC3C_4 | 4 | 8 | PF02991 | 0.173 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 562 | 568 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.632 |
LIG_MYND_1 | 427 | 431 | PF01753 | 0.564 |
LIG_Pex14_1 | 16 | 20 | PF04695 | 0.410 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.608 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 309 | 313 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 46 | 49 | PF00017 | 0.490 |
LIG_SH2_SRC | 618 | 621 | PF00017 | 0.586 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.486 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.661 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.689 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.599 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.552 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.641 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.610 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.552 |
LIG_SH3_5 | 42 | 46 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 4 | 10 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 482 | 488 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 384 | 390 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 561 | 573 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 71 | 77 | PF11976 | 0.523 |
LIG_TYR_ITIM | 272 | 277 | PF00017 | 0.233 |
LIG_TYR_ITSM | 305 | 312 | PF00017 | 0.361 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.523 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.418 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.581 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.687 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.410 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.552 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.347 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.616 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.488 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.415 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.537 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.344 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.229 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.659 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.587 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.431 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.401 |
MOD_Cter_Amidation | 671 | 674 | PF01082 | 0.479 |
MOD_Cter_Amidation | 93 | 96 | PF01082 | 0.532 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.496 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.467 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.483 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.571 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.323 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.489 |
MOD_GlcNHglycan | 659 | 663 | PF01048 | 0.278 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.474 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.546 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.776 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.487 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.441 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.541 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.400 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.374 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.397 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.525 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.421 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.258 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.566 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.526 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.366 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.546 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.402 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.564 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.486 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.532 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.328 |
MOD_PK_1 | 301 | 307 | PF00069 | 0.460 |
MOD_PKA_1 | 301 | 307 | PF00069 | 0.428 |
MOD_PKA_1 | 543 | 549 | PF00069 | 0.433 |
MOD_PKA_1 | 673 | 679 | PF00069 | 0.444 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.552 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.458 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.371 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.434 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.426 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.522 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.442 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.500 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.490 |
MOD_PKB_1 | 96 | 104 | PF00069 | 0.540 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.489 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.478 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.348 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.395 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.605 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.431 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.372 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.407 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.493 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.479 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.467 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.659 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.418 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.442 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.506 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.596 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.477 |
MOD_SUMO_rev_2 | 494 | 504 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 571 | 577 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 591 | 601 | PF00179 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.353 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 615 | 617 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAY3 | Leptomonas seymouri | 60% | 99% |
A0A1X0NUW5 | Trypanosomatidae | 33% | 100% |
A0A3S5H7R6 | Leishmania donovani | 92% | 100% |
A0A422N8N4 | Trypanosoma rangeli | 32% | 100% |
A4HK74 | Leishmania braziliensis | 79% | 100% |
A4I7Q9 | Leishmania infantum | 91% | 100% |
D0A9W4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q5I9 | Leishmania major | 91% | 100% |
V5BGK4 | Trypanosoma cruzi | 33% | 100% |