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 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBR8
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: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 | 1 |
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 | 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: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 | 383 | 387 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.391 |
CLV_PCSK_FUR_1 | 422 | 426 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.401 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.473 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.489 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.389 |
DOC_CYCLIN_RxL_1 | 264 | 272 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 63 | 69 | PF00134 | 0.423 |
DOC_MAPK_gen_1 | 290 | 296 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 397 | 407 | PF00069 | 0.437 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.300 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.320 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.246 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.685 |
DOC_USP7_MATH_2 | 347 | 353 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.586 |
LIG_Actin_WH2_2 | 348 | 363 | PF00022 | 0.322 |
LIG_Actin_WH2_2 | 378 | 396 | PF00022 | 0.466 |
LIG_APCC_ABBA_1 | 44 | 49 | PF00400 | 0.340 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.399 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.587 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.383 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.502 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.392 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.378 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.453 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.363 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.440 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.478 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.522 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.553 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.619 |
LIG_LIR_Apic_2 | 109 | 114 | PF02991 | 0.316 |
LIG_LIR_Apic_2 | 342 | 346 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 54 | 58 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 229 | 240 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.392 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.462 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.514 |
LIG_PCNA_PIPBox_1 | 423 | 432 | PF02747 | 0.429 |
LIG_PCNA_yPIPBox_3 | 419 | 430 | PF02747 | 0.403 |
LIG_PTB_Apo_2 | 425 | 432 | PF02174 | 0.480 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.514 |
LIG_SH2_PTP2 | 343 | 346 | PF00017 | 0.469 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 208 | 211 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.206 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.332 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.446 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.514 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.291 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.499 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.286 |
LIG_TRFH_1 | 343 | 347 | PF08558 | 0.486 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.484 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.319 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.704 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.644 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.312 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.527 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.490 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.431 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.501 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.390 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.271 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.700 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.550 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.533 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.368 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.428 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.660 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.685 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.737 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.671 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.487 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.386 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.452 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.667 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.587 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.332 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.686 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.622 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.359 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.368 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.468 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.431 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.569 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.308 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.516 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.599 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.214 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.479 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.663 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.516 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.351 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.450 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.474 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.380 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.436 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.416 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.360 |
MOD_OFUCOSY | 371 | 376 | PF10250 | 0.266 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.545 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.485 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.304 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.366 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.373 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.439 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.399 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.445 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.424 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.478 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.455 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.339 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.408 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.367 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.343 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.562 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.387 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.466 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.440 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.327 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.450 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.462 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.504 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.677 |
MOD_SUMO_rev_2 | 144 | 153 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 28 | 34 | PF00179 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.263 |
TRG_NES_CRM1_1 | 10 | 23 | PF08389 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 327 | 332 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL96 | Leptomonas seymouri | 55% | 100% |
A0A0S4IN59 | Bodo saltans | 32% | 100% |
A0A1X0NWW3 | Trypanosomatidae | 39% | 100% |
A0A422N8X4 | Trypanosoma rangeli | 39% | 100% |
A4HCV2 | Leishmania braziliensis | 78% | 100% |
A4I0D3 | Leishmania infantum | 99% | 100% |
C9ZV37 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AW97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QB81 | Leishmania major | 92% | 100% |
Q5ZIZ2 | Gallus gallus | 26% | 100% |
Q6GMV2 | Homo sapiens | 26% | 100% |
V5BBM7 | Trypanosoma cruzi | 37% | 100% |