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: A4H5W8
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 | 158 | 162 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.532 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.556 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.516 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 186 | 197 | PF00134 | 0.609 |
DOC_MAPK_DCC_7 | 342 | 351 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.521 |
DOC_MAPK_HePTP_8 | 126 | 138 | PF00069 | 0.412 |
DOC_MAPK_HePTP_8 | 339 | 351 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 129 | 138 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.481 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.685 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 283 | 293 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 476 | 484 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.434 |
LIG_APCC_ABBA_1 | 351 | 356 | PF00400 | 0.440 |
LIG_APCC_ABBAyCdc20_2 | 402 | 408 | PF00400 | 0.574 |
LIG_BIR_III_2 | 161 | 165 | PF00653 | 0.619 |
LIG_BIR_III_2 | 41 | 45 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 420 | 424 | PF00533 | 0.711 |
LIG_CtBP_PxDLS_1 | 389 | 395 | PF00389 | 0.562 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.508 |
LIG_deltaCOP1_diTrp_1 | 492 | 501 | PF00928 | 0.407 |
LIG_EH1_1 | 287 | 295 | PF00400 | 0.580 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.385 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.515 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.529 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.546 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.469 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.489 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.351 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.510 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.673 |
LIG_Pex14_1 | 495 | 499 | PF04695 | 0.400 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.718 |
LIG_SH2_NCK_1 | 396 | 400 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.630 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.494 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.498 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.580 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.636 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.594 |
LIG_SUMO_SIM_par_1 | 295 | 302 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 308 | 315 | PF11976 | 0.569 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.496 |
LIG_TRAF2_1 | 504 | 507 | PF00917 | 0.628 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.558 |
MOD_CDK_SPxK_1 | 3 | 9 | PF00069 | 0.469 |
MOD_CDK_SPxxK_3 | 465 | 472 | PF00069 | 0.754 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.571 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.590 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.627 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.657 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.538 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.679 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.708 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.703 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.661 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.498 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.633 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.618 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.347 |
MOD_GlcNHglycan | 320 | 325 | PF01048 | 0.355 |
MOD_GlcNHglycan | 418 | 423 | PF01048 | 0.751 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.733 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.610 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.516 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.459 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.494 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.683 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.512 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.761 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.715 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.500 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.476 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.715 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.292 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.822 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.398 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.411 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.621 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.532 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.606 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.482 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.461 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.500 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.667 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.529 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.619 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.527 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.584 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.644 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.537 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.587 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.710 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.519 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.480 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.602 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.569 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.570 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.532 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.560 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.516 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.652 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.536 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.659 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.773 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.709 |
MOD_SUMO_rev_2 | 15 | 24 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 413 | 422 | PF00179 | 0.686 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.597 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.610 |
TRG_NLS_MonoExtC_3 | 531 | 536 | PF00514 | 0.599 |
TRG_NLS_MonoExtN_4 | 531 | 536 | PF00514 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IB06 | Leptomonas seymouri | 62% | 99% |
A0A0S4JCA3 | Bodo saltans | 28% | 92% |
A0A1X0NHU4 | Trypanosomatidae | 37% | 100% |
A0A3S7WQW9 | Leishmania donovani | 82% | 100% |
A0A422NZM7 | Trypanosoma rangeli | 38% | 100% |
A4HU63 | Leishmania infantum | 82% | 100% |
D0A9P4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 95% |
E9AMZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QHN4 | Leishmania major | 82% | 100% |
V5AY09 | Trypanosoma cruzi | 39% | 100% |