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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8K3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.335 |
DEG_SCF_FBW7_1 | 290 | 296 | PF00400 | 0.514 |
DOC_CKS1_1 | 242 | 247 | PF01111 | 0.352 |
DOC_CKS1_1 | 290 | 295 | PF01111 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 331 | 337 | PF00134 | 0.364 |
DOC_MAPK_gen_1 | 208 | 218 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 327 | 335 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 336 | 343 | PF00149 | 0.424 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.368 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.378 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.330 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.503 |
LIG_Actin_WH2_2 | 247 | 262 | PF00022 | 0.368 |
LIG_CaM_IQ_9 | 268 | 283 | PF13499 | 0.389 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.435 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.447 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.439 |
LIG_LIR_Apic_2 | 241 | 245 | PF02991 | 0.367 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 14 | 21 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.360 |
LIG_PTB_Apo_2 | 133 | 140 | PF02174 | 0.414 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.405 |
LIG_SH3_1 | 351 | 357 | PF00018 | 0.420 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.539 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.454 |
LIG_SH3_5 | 238 | 242 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.422 |
LIG_TRFH_1 | 295 | 299 | PF08558 | 0.388 |
LIG_TRFH_1 | 58 | 62 | PF08558 | 0.372 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.547 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.446 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.519 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.461 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.476 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.575 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.571 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.319 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.399 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.426 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.356 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.332 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.322 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.517 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.434 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.399 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.397 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.304 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.508 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.402 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.480 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.356 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.452 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.444 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.378 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.548 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.342 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.375 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.429 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.532 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.513 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.330 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.417 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.340 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.460 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.487 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.340 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.376 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.423 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.427 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.559 |
MOD_SUMO_rev_2 | 204 | 211 | PF00179 | 0.720 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 276 | 281 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA55 | Leptomonas seymouri | 48% | 75% |
A0A3Q8IQE0 | Leishmania donovani | 89% | 71% |
A4HGA7 | Leishmania braziliensis | 74% | 100% |
A4I3E1 | Leishmania infantum | 89% | 100% |
E9AZM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |