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: Q4QC17
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.557 |
CLV_PCSK_PC7_1 | 22 | 28 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.448 |
DEG_MDM2_SWIB_1 | 169 | 177 | PF02201 | 0.476 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.459 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.526 |
DOC_CYCLIN_RxL_1 | 394 | 405 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 7 | 15 | PF00069 | 0.448 |
DOC_PP1_RVXF_1 | 83 | 90 | PF00149 | 0.466 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.503 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.452 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.542 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 316 | 321 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 301 | 318 | PF00022 | 0.459 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 171 | 179 | PF00928 | 0.488 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.376 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.458 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.427 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.549 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.544 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.529 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.535 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.280 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.262 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.524 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.448 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.522 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.542 |
LIG_LIR_Apic_2 | 74 | 80 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 229 | 238 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 276 | 286 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 64 | 73 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.382 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.486 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.462 |
LIG_Rb_pABgroove_1 | 147 | 155 | PF01858 | 0.360 |
LIG_REV1ctd_RIR_1 | 334 | 343 | PF16727 | 0.495 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.498 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.448 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.322 |
LIG_SUMO_SIM_anti_2 | 240 | 245 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 434 | 441 | PF11976 | 0.609 |
LIG_SUMO_SIM_par_1 | 207 | 213 | PF11976 | 0.469 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.421 |
MOD_CDK_SPxxK_3 | 309 | 316 | PF00069 | 0.445 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.491 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.474 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.484 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.350 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.498 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.631 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.562 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.499 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.547 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.464 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.562 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.374 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.452 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.493 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.564 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.608 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.464 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.482 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.418 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.541 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.397 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.413 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.607 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.563 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.553 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.520 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.426 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.509 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.476 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.368 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.285 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.452 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.312 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.433 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.537 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.439 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.422 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.502 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.540 |
MOD_PK_1 | 237 | 243 | PF00069 | 0.448 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.319 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.496 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.385 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.536 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.414 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.525 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.463 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.551 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.359 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.484 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.522 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.477 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.401 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.462 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.355 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.376 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.615 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.443 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.474 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.242 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.512 |
MOD_SUMO_rev_2 | 156 | 166 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 81 | 87 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_2 | 130 | 136 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.436 |
TRG_DiLeu_LyEn_5 | 189 | 194 | PF01217 | 0.465 |
TRG_ER_diArg_1 | 215 | 218 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 4 | 17 | PF08389 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 51 | 56 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1III8 | Leptomonas seymouri | 59% | 100% |
A0A1X0NJ75 | Trypanosomatidae | 35% | 100% |
A0A3Q8IC10 | Leishmania donovani | 93% | 100% |
A0A3S5IQQ3 | Trypanosoma rangeli | 34% | 100% |
A4HC29 | Leishmania braziliensis | 82% | 99% |
A4HZH2 | Leishmania infantum | 94% | 100% |
D0A102 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AVG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BRG3 | Trypanosoma cruzi | 34% | 100% |