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: A4HIG3
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_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.264 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.461 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.497 |
CLV_PCSK_FUR_1 | 238 | 242 | PF00082 | 0.484 |
CLV_PCSK_FUR_1 | 248 | 252 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 55 | 57 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 31 | 37 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.514 |
CLV_Separin_Metazoa | 338 | 342 | PF03568 | 0.386 |
DEG_APCC_DBOX_1 | 391 | 399 | PF00400 | 0.375 |
DOC_CKS1_1 | 183 | 188 | PF01111 | 0.350 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.414 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 37 | 45 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 165 | 168 | PF00134 | 0.320 |
DOC_MAPK_DCC_7 | 164 | 172 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 248 | 255 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 35 | 43 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 67 | 74 | PF00069 | 0.356 |
DOC_MAPK_HePTP_8 | 64 | 76 | PF00069 | 0.256 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.319 |
DOC_MAPK_RevD_3 | 21 | 36 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 407 | 413 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.320 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.321 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.349 |
LIG_14-3-3_CanoR_1 | 193 | 197 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.480 |
LIG_AP2alpha_1 | 144 | 148 | PF02296 | 0.425 |
LIG_APCC_ABBA_1 | 145 | 150 | PF00400 | 0.440 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_2 | 49 | 55 | PF00533 | 0.356 |
LIG_DLG_GKlike_1 | 68 | 76 | PF00625 | 0.265 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.358 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.366 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.565 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.432 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.527 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.459 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.575 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.486 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.399 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.321 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.416 |
LIG_KLC1_Yacidic_2 | 319 | 324 | PF13176 | 0.328 |
LIG_LIR_Apic_2 | 213 | 219 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 417 | 423 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 142 | 152 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 333 | 344 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.342 |
LIG_LYPXL_yS_3 | 422 | 425 | PF13949 | 0.285 |
LIG_PDZ_Class_1 | 459 | 464 | PF00595 | 0.474 |
LIG_Pex14_2 | 144 | 148 | PF04695 | 0.425 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.474 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.320 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.410 |
LIG_SH2_SRC | 207 | 210 | PF00017 | 0.453 |
LIG_SH2_SRC | 79 | 82 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.479 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.355 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.463 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.383 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.332 |
LIG_SUMO_SIM_anti_2 | 353 | 358 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 251 | 257 | PF11976 | 0.404 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.446 |
LIG_TRFH_1 | 422 | 426 | PF08558 | 0.284 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.452 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.565 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.461 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.375 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.460 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.425 |
MOD_Cter_Amidation | 248 | 251 | PF01082 | 0.421 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.424 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.361 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.507 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.433 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.521 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.360 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.422 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.500 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.512 |
MOD_LATS_1 | 326 | 332 | PF00433 | 0.403 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.398 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.317 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.501 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.400 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.422 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.536 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.568 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.329 |
MOD_PK_1 | 414 | 420 | PF00069 | 0.476 |
MOD_PK_1 | 456 | 462 | PF00069 | 0.463 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.516 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.479 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.263 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.421 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.426 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.493 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.502 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.340 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.398 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.442 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.411 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.348 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.456 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.477 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.349 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.412 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.445 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.364 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.306 |
MOD_SUMO_for_1 | 54 | 57 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 378 | 384 | PF00179 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 420 | 425 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.285 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 393 | 397 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P922 | Leptomonas seymouri | 73% | 100% |
A0A1X0P2C1 | Trypanosomatidae | 47% | 100% |
A0A3S7X3J4 | Leishmania donovani | 87% | 100% |
A0A422NW63 | Trypanosoma rangeli | 48% | 100% |
A4I5Q9 | Leishmania infantum | 87% | 100% |
C9ZR28 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B104 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q762 | Leishmania major | 88% | 100% |
V5BGV8 | Trypanosoma cruzi | 46% | 100% |