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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AMZ3
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:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 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: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:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.538 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.648 |
DOC_CYCLIN_RxL_1 | 185 | 196 | PF00134 | 0.616 |
DOC_MAPK_DCC_7 | 341 | 350 | PF00069 | 0.538 |
DOC_MAPK_HePTP_8 | 125 | 137 | PF00069 | 0.403 |
DOC_MAPK_HePTP_8 | 338 | 350 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 341 | 350 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 488 | 495 | PF00149 | 0.276 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.513 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 282 | 292 | PF00244 | 0.541 |
LIG_Actin_WH2_2 | 10 | 28 | PF00022 | 0.316 |
LIG_APCC_ABBA_1 | 350 | 355 | PF00400 | 0.440 |
LIG_APCC_ABBAyCdc20_2 | 401 | 407 | PF00400 | 0.576 |
LIG_BIR_III_2 | 160 | 164 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 471 | 475 | PF00533 | 0.796 |
LIG_CtBP_PxDLS_1 | 388 | 394 | PF00389 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 491 | 500 | PF00928 | 0.403 |
LIG_EH1_1 | 286 | 294 | PF00400 | 0.534 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.386 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.515 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.521 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.490 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.469 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.458 |
LIG_LIR_Gen_1 | 61 | 68 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.283 |
LIG_Pex14_1 | 494 | 498 | PF04695 | 0.392 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.356 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.286 |
LIG_SH2_GRB2like | 32 | 35 | PF00017 | 0.718 |
LIG_SH2_GRB2like | 561 | 564 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.361 |
LIG_SH3_2 | 151 | 156 | PF14604 | 0.335 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.498 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.503 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.580 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.737 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.669 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.622 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.562 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.496 |
LIG_TYR_ITIM | 62 | 67 | PF00017 | 0.286 |
MOD_CDC14_SPxK_1 | 153 | 156 | PF00782 | 0.518 |
MOD_CDK_SPxK_1 | 150 | 156 | PF00069 | 0.544 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.567 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.558 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.620 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.683 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.693 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.547 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.619 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.303 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.549 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.619 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.592 |
MOD_GlcNHglycan | 320 | 324 | PF01048 | 0.443 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.382 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.725 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.586 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.530 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.375 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.678 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.516 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.736 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.565 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.550 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.721 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.351 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.397 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.415 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.617 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.620 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.307 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.363 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.652 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.565 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.582 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.534 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.592 |
MOD_PK_1 | 63 | 69 | PF00069 | 0.487 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.580 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.637 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.544 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.561 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.530 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.558 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.552 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.396 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.654 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.487 |
MOD_PKB_1 | 469 | 477 | PF00069 | 0.503 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.459 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.565 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.447 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.541 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.522 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.546 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.642 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.663 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.551 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.761 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 14 | 23 | PF00179 | 0.498 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.619 |
TRG_NLS_MonoExtC_3 | 530 | 535 | PF00514 | 0.599 |
TRG_NLS_MonoExtN_4 | 530 | 535 | PF00514 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IB06 | Leptomonas seymouri | 60% | 99% |
A0A0S4JCA3 | Bodo saltans | 28% | 91% |
A0A1X0NHU4 | Trypanosomatidae | 38% | 100% |
A0A3S7WQW9 | Leishmania donovani | 91% | 100% |
A0A422NZM7 | Trypanosoma rangeli | 39% | 100% |
A4H5W8 | Leishmania braziliensis | 80% | 100% |
A4HU63 | Leishmania infantum | 91% | 100% |
D0A9P4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 95% |
Q4QHN4 | Leishmania major | 91% | 100% |
V5AY09 | Trypanosoma cruzi | 38% | 100% |