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: A0A3Q8IFW4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.403 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.388 |
CLV_PCSK_FUR_1 | 458 | 462 | PF00082 | 0.466 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.439 |
CLV_Separin_Metazoa | 61 | 65 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.399 |
DEG_APCC_KENBOX_2 | 356 | 360 | PF00400 | 0.399 |
DOC_CYCLIN_yClb1_LxF_4 | 448 | 454 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 144 | 152 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 262 | 270 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 385 | 393 | PF00069 | 0.492 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.507 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 208 | 217 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 218 | 226 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 292 | 296 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 433 | 440 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 92 | 98 | PF00244 | 0.532 |
LIG_CaM_IQ_9 | 77 | 93 | PF13499 | 0.413 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.518 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.513 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.653 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.500 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.390 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.517 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 245 | 253 | PF00786 | 0.526 |
LIG_LIR_Gen_1 | 12 | 21 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 369 | 376 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.510 |
LIG_NRBOX | 346 | 352 | PF00104 | 0.493 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.459 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.545 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.684 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.489 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.516 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.522 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.513 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.401 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.560 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.544 |
LIG_UBA3_1 | 199 | 205 | PF00899 | 0.444 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.440 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.443 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.454 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.561 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.538 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.548 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.624 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.371 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.475 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.391 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.531 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.522 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.455 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.466 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.493 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.514 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.650 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.683 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.447 |
MOD_GlcNHglycan | 26 | 30 | PF01048 | 0.524 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.499 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.404 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.477 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.473 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.589 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.516 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.674 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.409 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.462 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.405 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.542 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.485 |
MOD_N-GLC_2 | 133 | 135 | PF02516 | 0.582 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.505 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.505 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.498 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.539 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.515 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.454 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.452 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.514 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.410 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.354 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.514 |
MOD_PKA_1 | 460 | 466 | PF00069 | 0.505 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.416 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.480 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.510 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.477 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.468 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.500 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.544 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.497 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.582 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.549 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.508 |
MOD_Plk_2-3 | 9 | 15 | PF00069 | 0.466 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.482 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.531 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.505 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.548 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.531 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.540 |
MOD_SUMO_for_1 | 6 | 9 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 232 | 237 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 223 | 228 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.389 |
TRG_NLS_MonoCore_2 | 263 | 268 | PF00514 | 0.486 |
TRG_NLS_MonoExtC_3 | 203 | 208 | PF00514 | 0.444 |
TRG_NLS_MonoExtN_4 | 204 | 209 | PF00514 | 0.399 |
TRG_NLS_MonoExtN_4 | 262 | 269 | PF00514 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 208 | 213 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 282 | 287 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9S1 | Leptomonas seymouri | 25% | 100% |
A4HCY5 | Leishmania braziliensis | 69% | 100% |
A4I0H0 | Leishmania infantum | 98% | 100% |
E9AWD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QB40 | Leishmania major | 90% | 100% |