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: A4H616
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 458 | 462 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.741 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.801 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 361 | 365 | PF03568 | 0.477 |
DEG_APCC_DBOX_1 | 131 | 139 | PF00400 | 0.540 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.399 |
DOC_CYCLIN_yCln2_LP_2 | 209 | 212 | PF00134 | 0.321 |
DOC_MAPK_MEF2A_6 | 336 | 345 | PF00069 | 0.529 |
DOC_MAPK_NFAT4_5 | 336 | 344 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.321 |
DOC_PP4_FxxP_1 | 90 | 93 | PF00568 | 0.419 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.590 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 205 | 212 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 364 | 374 | PF00244 | 0.487 |
LIG_Actin_WH2_2 | 189 | 207 | PF00022 | 0.485 |
LIG_Actin_WH2_2 | 356 | 373 | PF00022 | 0.574 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.331 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.531 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.427 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.534 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.568 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.417 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.575 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.343 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.413 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.557 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.464 |
LIG_GBD_Chelix_1 | 331 | 339 | PF00786 | 0.521 |
LIG_HP1_1 | 9 | 13 | PF01393 | 0.338 |
LIG_LIR_Apic_2 | 87 | 93 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 215 | 223 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.511 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.461 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.467 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.533 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.662 |
LIG_SUMO_SIM_anti_2 | 141 | 146 | PF11976 | 0.291 |
LIG_SUMO_SIM_anti_2 | 359 | 365 | PF11976 | 0.556 |
LIG_SUMO_SIM_anti_2 | 393 | 398 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 171 | 177 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.410 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.575 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.555 |
MOD_CDK_SPK_2 | 435 | 440 | PF00069 | 0.719 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.727 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.454 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.550 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.499 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.663 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.616 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.562 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.476 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.397 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.490 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.581 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.614 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.345 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.764 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.388 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.530 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.729 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.621 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.449 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.488 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.525 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.642 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.492 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.525 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.609 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.710 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.535 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.563 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.738 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.711 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.484 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.495 |
MOD_LATS_1 | 410 | 416 | PF00433 | 0.485 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.545 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.395 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.471 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.515 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.398 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.502 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.538 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.625 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.525 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.443 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.469 |
MOD_NEK2_2 | 3 | 8 | PF00069 | 0.345 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.502 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.421 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.727 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.465 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.621 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.676 |
MOD_PKB_1 | 291 | 299 | PF00069 | 0.515 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.466 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.490 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.449 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.359 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.414 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.558 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.611 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.577 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.527 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.529 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.476 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.639 |
MOD_SUMO_for_1 | 182 | 185 | PF00179 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 337 | 342 | PF01217 | 0.444 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.482 |
TRG_NES_CRM1_1 | 395 | 406 | PF08389 | 0.524 |
TRG_NLS_Bipartite_1 | 162 | 184 | PF00514 | 0.515 |
TRG_NLS_MonoExtC_3 | 179 | 185 | PF00514 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC0 | Leptomonas seymouri | 34% | 87% |
A0A3Q8I7N0 | Leishmania donovani | 69% | 100% |
A4HUE3 | Leishmania infantum | 69% | 100% |
E9AN43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4QHI3 | Leishmania major | 68% | 100% |