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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A4HTM8
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 3 |
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 | 3 |
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 | 3 |
GO:0008168 | methyltransferase activity | 4 | 3 |
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 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
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 | 23 | 27 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.713 |
CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.470 |
DEG_APCC_DBOX_1 | 184 | 192 | PF00400 | 0.532 |
DEG_SCF_TRCP1_1 | 148 | 154 | PF00400 | 0.539 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.693 |
DEG_SPOP_SBC_1 | 276 | 280 | PF00917 | 0.613 |
DEG_SPOP_SBC_1 | 434 | 438 | PF00917 | 0.563 |
DEG_SPOP_SBC_1 | 441 | 445 | PF00917 | 0.524 |
DOC_CYCLIN_RxL_1 | 484 | 491 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 28 | 40 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 347 | 355 | PF00069 | 0.510 |
DOC_PP2B_LxvP_1 | 137 | 140 | PF13499 | 0.486 |
DOC_PP2B_PxIxI_1 | 50 | 56 | PF00149 | 0.446 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.460 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.766 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 403 | 412 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 421 | 431 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 432 | 442 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 494 | 503 | PF00244 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.742 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.534 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.583 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.371 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.535 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.522 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.578 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.496 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.500 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.557 |
LIG_LIR_Apic_2 | 126 | 130 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 337 | 346 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 469 | 478 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.417 |
LIG_NRP_CendR_1 | 509 | 510 | PF00754 | 0.581 |
LIG_Rb_pABgroove_1 | 382 | 390 | PF01858 | 0.540 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.509 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.490 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 388 | 392 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.656 |
LIG_SH2_PTP2 | 472 | 475 | PF00017 | 0.421 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.430 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 52 | 58 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 383 | 390 | PF11976 | 0.546 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.607 |
LIG_TRAF2_1 | 464 | 467 | PF00917 | 0.467 |
LIG_TYR_ITIM | 470 | 475 | PF00017 | 0.552 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.467 |
LIG_WW_1 | 331 | 334 | PF00397 | 0.502 |
LIG_WW_3 | 330 | 334 | PF00397 | 0.530 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.395 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.733 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.701 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.593 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.527 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.569 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.587 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.518 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.607 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.708 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.789 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.485 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.351 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.642 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.578 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.410 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.665 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.606 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.352 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.466 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.572 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.489 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.793 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.504 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.556 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.267 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.509 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.382 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.380 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.516 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.563 |
MOD_OFUCOSY | 372 | 378 | PF10250 | 0.267 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.510 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.714 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.487 |
MOD_PK_1 | 177 | 183 | PF00069 | 0.659 |
MOD_PK_1 | 349 | 355 | PF00069 | 0.485 |
MOD_PKA_1 | 422 | 428 | PF00069 | 0.557 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.696 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.211 |
MOD_PKB_1 | 347 | 355 | PF00069 | 0.546 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.567 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.485 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.476 |
MOD_Plk_2-3 | 474 | 480 | PF00069 | 0.586 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.640 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.428 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.697 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.551 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.553 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.374 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.765 |
TRG_DiLeu_BaEn_2 | 490 | 496 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 319 | 322 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.524 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.678 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.701 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I8 | Leptomonas seymouri | 49% | 92% |
A0A1X0NPE5 | Trypanosomatidae | 26% | 100% |
A0A3S5H671 | Leishmania donovani | 100% | 79% |
A0A3S5IRB9 | Trypanosoma rangeli | 29% | 100% |
A4H6C5 | Leishmania braziliensis | 84% | 99% |
C9ZPC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AMG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QI81 | Leishmania major | 94% | 100% |