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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QI81
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016571 | histone methylation | 5 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 3 |
GO:0034968 | histone lysine methylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.360 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.720 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.526 |
DEG_APCC_DBOX_1 | 190 | 198 | PF00400 | 0.582 |
DEG_SCF_TRCP1_1 | 154 | 160 | PF00400 | 0.556 |
DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 445 | 449 | PF00917 | 0.531 |
DOC_CYCLIN_RxL_1 | 488 | 495 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 34 | 46 | PF00069 | 0.662 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.511 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.548 |
DOC_PP2B_PxIxI_1 | 56 | 62 | PF00149 | 0.495 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.477 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 271 | 277 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 436 | 446 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 498 | 507 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.426 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.542 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.721 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.424 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.544 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.588 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.503 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.598 |
LIG_LIR_Apic_2 | 8 | 13 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 341 | 345 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 495 | 500 | PF02991 | 0.434 |
LIG_NRP_CendR_1 | 513 | 514 | PF00754 | 0.602 |
LIG_Rb_pABgroove_1 | 386 | 394 | PF01858 | 0.554 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.559 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.506 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 392 | 396 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 10 | 13 | PF00017 | 0.692 |
LIG_SH2_PTP2 | 476 | 479 | PF00017 | 0.454 |
LIG_SH2_SRC | 10 | 13 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.443 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.451 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.591 |
LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 387 | 394 | PF11976 | 0.530 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.612 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.501 |
LIG_TYR_ITIM | 474 | 479 | PF00017 | 0.586 |
LIG_WRC_WIRS_1 | 273 | 278 | PF05994 | 0.503 |
LIG_WW_1 | 335 | 338 | PF00397 | 0.560 |
LIG_WW_3 | 334 | 338 | PF00397 | 0.598 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.470 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.733 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.598 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.536 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.585 |
MOD_Cter_Amidation | 180 | 183 | PF01082 | 0.650 |
MOD_Cter_Amidation | 36 | 39 | PF01082 | 0.612 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.562 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.648 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.769 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.788 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.497 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.341 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.803 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.659 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.575 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.463 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.706 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.494 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.470 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.457 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.558 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.489 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.526 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.528 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.301 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.721 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.554 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.418 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.493 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.560 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.560 |
MOD_OFUCOSY | 376 | 382 | PF10250 | 0.301 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.766 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.542 |
MOD_PK_1 | 183 | 189 | PF00069 | 0.700 |
MOD_PK_1 | 353 | 359 | PF00069 | 0.510 |
MOD_PKA_1 | 426 | 432 | PF00069 | 0.562 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.738 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.362 |
MOD_PKB_1 | 351 | 359 | PF00069 | 0.560 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.617 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.525 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.501 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.627 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.644 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.542 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.537 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.773 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.699 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.259 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.564 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.566 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.434 |
TRG_DiLeu_BaEn_2 | 494 | 500 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 170 | 175 | PF01217 | 0.593 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.569 |
TRG_NLS_MonoExtC_3 | 33 | 38 | PF00514 | 0.694 |
TRG_NLS_MonoExtN_4 | 31 | 38 | PF00514 | 0.746 |
TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 73 | 78 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I8 | Leptomonas seymouri | 49% | 93% |
A0A1X0NPE5 | Trypanosomatidae | 26% | 100% |
A0A3S5H671 | Leishmania donovani | 94% | 79% |
A4H6C5 | Leishmania braziliensis | 86% | 100% |
A4HTM8 | Leishmania infantum | 94% | 100% |
C9ZPC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AMG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |