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: A4H7V8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.320 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 266 | 272 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 109 | 113 | PF03568 | 0.353 |
CLV_Separin_Metazoa | 250 | 254 | PF03568 | 0.335 |
CLV_Separin_Metazoa | 308 | 312 | PF03568 | 0.523 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.481 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.513 |
DOC_ANK_TNKS_1 | 43 | 50 | PF00023 | 0.519 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.528 |
DOC_CYCLIN_RxL_1 | 184 | 194 | PF00134 | 0.354 |
DOC_CYCLIN_RxL_1 | 199 | 207 | PF00134 | 0.399 |
DOC_CYCLIN_RxL_1 | 53 | 63 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 189 | 195 | PF00134 | 0.417 |
DOC_CYCLIN_yCln2_LP_2 | 45 | 48 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 156 | 164 | PF00069 | 0.489 |
DOC_MAPK_RevD_3 | 258 | 271 | PF00069 | 0.403 |
DOC_MIT_MIM_1 | 181 | 189 | PF04212 | 0.276 |
DOC_PP1_RVXF_1 | 279 | 286 | PF00149 | 0.398 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.524 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 381 | 384 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.517 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 317 | 324 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 86 | 94 | PF00244 | 0.480 |
LIG_14-3-3_CterR_2 | 413 | 416 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 261 | 279 | PF00022 | 0.320 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.306 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.501 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.392 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.354 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.486 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.619 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.611 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.517 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.404 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.753 |
LIG_Integrin_RGD_1 | 168 | 170 | PF01839 | 0.326 |
LIG_LIR_Apic_2 | 379 | 384 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 140 | 151 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 241 | 252 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.403 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.401 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.430 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.434 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.609 |
LIG_SH3_2 | 66 | 71 | PF14604 | 0.523 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.332 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.452 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.561 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.594 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.587 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.301 |
LIG_SUMO_SIM_anti_2 | 191 | 197 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.301 |
LIG_TYR_ITIM | 210 | 215 | PF00017 | 0.430 |
LIG_WRC_WIRS_1 | 262 | 267 | PF05994 | 0.361 |
LIG_WW_3 | 53 | 57 | PF00397 | 0.498 |
MOD_CDC14_SPxK_1 | 379 | 382 | PF00782 | 0.526 |
MOD_CDK_SPxK_1 | 376 | 382 | PF00069 | 0.518 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.435 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.365 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.658 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.448 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.563 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.529 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.427 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.368 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.388 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.517 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.545 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.466 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.636 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.626 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.325 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.503 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.597 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.578 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.571 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.472 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.528 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.345 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.545 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.388 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.500 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.454 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.454 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.577 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.418 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.459 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.567 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.554 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.625 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.506 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.399 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.381 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.454 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.459 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.468 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.378 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.483 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.591 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.490 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.573 |
TRG_AP2beta_CARGO_1 | 161 | 171 | PF09066 | 0.384 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.294 |
TRG_DiLeu_BaEn_2 | 140 | 146 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q5 | Leptomonas seymouri | 42% | 99% |
A0A3Q8I8Y2 | Leishmania donovani | 69% | 100% |
A4HW84 | Leishmania infantum | 69% | 100% |
E9APY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4QFJ6 | Leishmania major | 70% | 100% |