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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QB81
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
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 | 2 |
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 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
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 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
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 | 139 | 143 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.257 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.425 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 322 | 330 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 348 | 354 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 455 | 465 | PF00069 | 0.461 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.332 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.330 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.438 |
DOC_USP7_MATH_2 | 405 | 411 | PF00917 | 0.522 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 163 | 168 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 331 | 338 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 436 | 454 | PF00022 | 0.532 |
LIG_APCC_ABBA_1 | 101 | 106 | PF00400 | 0.406 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.403 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.407 |
LIG_EVH1_2 | 42 | 46 | PF00568 | 0.416 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.670 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.415 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.518 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.419 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.389 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.518 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.445 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.450 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.399 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.644 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.631 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.389 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.535 |
LIG_LIR_Apic_2 | 111 | 115 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 166 | 171 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 400 | 404 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.418 |
LIG_NRBOX | 323 | 329 | PF00104 | 0.480 |
LIG_NRBOX | 422 | 428 | PF00104 | 0.528 |
LIG_PCNA_PIPBox_1 | 481 | 490 | PF02747 | 0.455 |
LIG_PCNA_yPIPBox_3 | 477 | 488 | PF02747 | 0.434 |
LIG_PTB_Apo_2 | 483 | 490 | PF02174 | 0.497 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.528 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.532 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.371 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.322 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.491 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.406 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 294 | 301 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 461 | 466 | PF11976 | 0.532 |
LIG_TRFH_1 | 401 | 405 | PF08558 | 0.532 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.506 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.417 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.300 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.734 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.581 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.438 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.527 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.502 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.503 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.518 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.707 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.628 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.396 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.439 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.501 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.690 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.747 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.695 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.559 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.410 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.530 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.274 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.488 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.540 |
MOD_GlcNHglycan | 9 | 13 | PF01048 | 0.406 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.633 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.370 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.703 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.660 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.374 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.433 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.429 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.452 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.387 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.455 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.589 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.344 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.234 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.464 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.448 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.489 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.397 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.433 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.391 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.418 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.471 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.487 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.398 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.397 |
MOD_OFUCOSY | 429 | 434 | PF10250 | 0.332 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.431 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.613 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.495 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.380 |
MOD_PKA_1 | 348 | 354 | PF00069 | 0.457 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.520 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.430 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.532 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.460 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.427 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.496 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.468 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.372 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.422 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.520 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.387 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.555 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.435 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.534 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.470 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.476 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.515 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.693 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.399 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.546 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.459 |
MOD_SUMO_rev_2 | 205 | 210 | PF00179 | 0.667 |
MOD_SUMO_rev_2 | 85 | 91 | PF00179 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.347 |
TRG_NES_CRM1_1 | 67 | 80 | PF08389 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 325 | 330 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 385 | 390 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL96 | Leptomonas seymouri | 54% | 100% |
A0A0S4IN59 | Bodo saltans | 30% | 100% |
A0A1X0NWW3 | Trypanosomatidae | 38% | 100% |
A0A3Q8IBR8 | Leishmania donovani | 92% | 100% |
A0A422N8X4 | Trypanosoma rangeli | 39% | 100% |
A4HCV2 | Leishmania braziliensis | 77% | 100% |
A4I0D3 | Leishmania infantum | 92% | 100% |
C9ZV37 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AW97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q6GMV2 | Homo sapiens | 25% | 100% |
V5BBM7 | Trypanosoma cruzi | 38% | 100% |