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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4I5Q9
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.470 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.503 |
CLV_PCSK_FUR_1 | 238 | 242 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.270 |
CLV_PCSK_PC7_1 | 31 | 37 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 338 | 342 | PF03568 | 0.391 |
DEG_SCF_FBW7_1 | 196 | 202 | PF00400 | 0.538 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.486 |
DOC_CKS1_1 | 165 | 170 | PF01111 | 0.333 |
DOC_CKS1_1 | 183 | 188 | PF01111 | 0.349 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.421 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 37 | 45 | PF00134 | 0.446 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 248 | 255 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 35 | 43 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.372 |
DOC_MAPK_NFAT4_5 | 405 | 413 | PF00069 | 0.374 |
DOC_MAPK_RevD_3 | 21 | 36 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 407 | 413 | PF00149 | 0.427 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.579 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 449 | 458 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 69 | 86 | PF00022 | 0.277 |
LIG_AP2alpha_1 | 144 | 148 | PF02296 | 0.422 |
LIG_APCC_ABBA_1 | 145 | 150 | PF00400 | 0.436 |
LIG_BRCT_BRCA1_1 | 102 | 106 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.351 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.430 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.362 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.399 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.363 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.572 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.436 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.532 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.568 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.481 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.399 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.356 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.417 |
LIG_KLC1_Yacidic_2 | 319 | 324 | PF13176 | 0.330 |
LIG_LIR_Apic_2 | 213 | 219 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 445 | 451 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 142 | 152 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 333 | 344 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.345 |
LIG_Pex14_2 | 144 | 148 | PF04695 | 0.422 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.484 |
LIG_REV1ctd_RIR_1 | 104 | 114 | PF16727 | 0.328 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.324 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.408 |
LIG_SH2_SRC | 207 | 210 | PF00017 | 0.449 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.479 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.454 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.386 |
LIG_SUMO_SIM_par_1 | 251 | 257 | PF11976 | 0.403 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.449 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.450 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.569 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.459 |
MOD_Cter_Amidation | 248 | 251 | PF01082 | 0.426 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.361 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.505 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.438 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.528 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.438 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.440 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.358 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.458 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.551 |
MOD_LATS_1 | 326 | 332 | PF00433 | 0.405 |
MOD_LATS_1 | 455 | 461 | PF00433 | 0.511 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.397 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.410 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.502 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.405 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.461 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.414 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.544 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.570 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.334 |
MOD_PK_1 | 414 | 420 | PF00069 | 0.479 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.517 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.420 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.426 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.430 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.489 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.452 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.337 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.398 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.442 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.340 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.409 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.353 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.466 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.334 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.348 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.416 |
MOD_SUMO_rev_2 | 380 | 384 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 420 | 425 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.501 |
TRG_NLS_Bipartite_1 | 373 | 395 | PF00514 | 0.433 |
TRG_NLS_MonoExtC_3 | 455 | 461 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 389 | 395 | PF00514 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 393 | 397 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P922 | Leptomonas seymouri | 72% | 100% |
A0A1X0P2C1 | Trypanosomatidae | 48% | 100% |
A0A3S7X3J4 | Leishmania donovani | 100% | 100% |
A0A422NW63 | Trypanosoma rangeli | 48% | 100% |
A4HIG3 | Leishmania braziliensis | 87% | 100% |
C9ZR28 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B104 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q762 | Leishmania major | 94% | 100% |
V5BGV8 | Trypanosoma cruzi | 45% | 100% |