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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H671
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.679 |
CLV_PCSK_PC7_1 | 311 | 317 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.495 |
DEG_SCF_TRCP1_1 | 287 | 293 | PF00400 | 0.525 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.588 |
DEG_SPOP_SBC_1 | 415 | 419 | PF00917 | 0.517 |
DEG_SPOP_SBC_1 | 573 | 577 | PF00917 | 0.503 |
DEG_SPOP_SBC_1 | 580 | 584 | PF00917 | 0.453 |
DOC_ANK_TNKS_1 | 51 | 58 | PF00023 | 0.499 |
DOC_CYCLIN_RxL_1 | 623 | 630 | PF00134 | 0.401 |
DOC_MAPK_gen_1 | 167 | 179 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 486 | 494 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 24 | 33 | PF00069 | 0.469 |
DOC_MAPK_NFAT4_5 | 24 | 32 | PF00069 | 0.469 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.458 |
DOC_PP2B_PxIxI_1 | 189 | 195 | PF00149 | 0.415 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.477 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 377 | 383 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 472 | 478 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 542 | 551 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 560 | 570 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 571 | 581 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 633 | 642 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.454 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.426 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.475 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.429 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.606 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.378 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.539 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.533 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.389 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.498 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.535 |
LIG_LIR_Apic_2 | 141 | 146 | PF02991 | 0.624 |
LIG_LIR_Apic_2 | 15 | 20 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 123 | 131 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 608 | 617 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.452 |
LIG_NRP_CendR_1 | 648 | 649 | PF00754 | 0.560 |
LIG_Pex14_2 | 87 | 91 | PF04695 | 0.461 |
LIG_Rb_pABgroove_1 | 521 | 529 | PF01858 | 0.470 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.454 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.468 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.382 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.391 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.517 |
LIG_SH2_PTP2 | 143 | 146 | PF00017 | 0.627 |
LIG_SH2_PTP2 | 611 | 614 | PF00017 | 0.415 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.415 |
LIG_SH3_2 | 89 | 94 | PF14604 | 0.458 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.488 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.550 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 191 | 197 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 522 | 529 | PF11976 | 0.502 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.504 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.477 |
LIG_TYR_ITIM | 609 | 614 | PF00017 | 0.540 |
LIG_WRC_WIRS_1 | 406 | 411 | PF05994 | 0.416 |
LIG_WW_1 | 470 | 473 | PF00397 | 0.395 |
LIG_WW_3 | 469 | 473 | PF00397 | 0.488 |
LIG_WW_3 | 58 | 62 | PF00397 | 0.462 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.463 |
MOD_CDK_SPxK_1 | 18 | 24 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 194 | 201 | PF00069 | 0.452 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.463 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.630 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.686 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.521 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.477 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.427 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.514 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.520 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.466 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.471 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.566 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.670 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.719 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.452 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.352 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.476 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.437 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.412 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.723 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.552 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.574 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.403 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.579 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.514 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.386 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.375 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.583 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.460 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.455 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.400 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.531 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.293 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.453 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.461 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.379 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.409 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.491 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.484 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.464 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.478 |
MOD_OFUCOSY | 511 | 517 | PF10250 | 0.277 |
MOD_OFUCOSY | 62 | 68 | PF10250 | 0.455 |
MOD_OFUCOSY | 95 | 102 | PF10250 | 0.474 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.678 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.410 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.499 |
MOD_PIKK_1 | 643 | 649 | PF00454 | 0.466 |
MOD_PK_1 | 120 | 126 | PF00069 | 0.464 |
MOD_PK_1 | 316 | 322 | PF00069 | 0.622 |
MOD_PK_1 | 488 | 494 | PF00069 | 0.489 |
MOD_PKA_1 | 561 | 567 | PF00069 | 0.535 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.451 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.646 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.509 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.262 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.440 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.468 |
MOD_PKB_1 | 486 | 494 | PF00069 | 0.402 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.526 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.493 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.477 |
MOD_Plk_2-3 | 613 | 619 | PF00069 | 0.537 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.467 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.525 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.557 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.459 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.459 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.381 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.669 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.589 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.483 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.487 |
TRG_DiLeu_BaEn_2 | 629 | 635 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 642 | 645 | PF00400 | 0.480 |
TRG_NLS_MonoExtC_3 | 166 | 171 | PF00514 | 0.565 |
TRG_NLS_MonoExtN_4 | 164 | 171 | PF00514 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 626 | 630 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I8 | Leptomonas seymouri | 49% | 100% |
A4H6C5 | Leishmania braziliensis | 84% | 99% |
A4HTM8 | Leishmania infantum | 100% | 100% |
E9AMG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QI81 | Leishmania major | 94% | 100% |