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: Q4QAX5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.356 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.349 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.530 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.265 |
DEG_APCC_DBOX_1 | 23 | 31 | PF00400 | 0.578 |
DEG_MDM2_SWIB_1 | 189 | 196 | PF02201 | 0.361 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.545 |
DEG_SCF_FBW7_1 | 71 | 76 | PF00400 | 0.512 |
DOC_CKS1_1 | 37 | 42 | PF01111 | 0.554 |
DOC_CYCLIN_RxL_1 | 134 | 144 | PF00134 | 0.456 |
DOC_CYCLIN_RxL_1 | 165 | 175 | PF00134 | 0.381 |
DOC_CYCLIN_RxL_1 | 260 | 270 | PF00134 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 139 | 145 | PF00134 | 0.267 |
DOC_MAPK_DCC_7 | 225 | 235 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 216 | 223 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 292 | 300 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 135 | 142 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 156 | 162 | PF00149 | 0.449 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.458 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.608 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 140 | 149 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 283 | 288 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 399 | 407 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 457 | 462 | PF00244 | 0.405 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.555 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.323 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.503 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.469 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.384 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.341 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.672 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.578 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.518 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.394 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.490 |
LIG_GBD_Chelix_1 | 424 | 432 | PF00786 | 0.449 |
LIG_GBD_Chelix_1 | 82 | 90 | PF00786 | 0.584 |
LIG_LIR_Apic_2 | 249 | 254 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 252 | 261 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.313 |
LIG_NRBOX | 194 | 200 | PF00104 | 0.459 |
LIG_OCRL_FandH_1 | 288 | 300 | PF00620 | 0.464 |
LIG_Pex14_2 | 189 | 193 | PF04695 | 0.368 |
LIG_Pex14_2 | 354 | 358 | PF04695 | 0.413 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.474 |
LIG_SH2_CRK | 435 | 439 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.359 |
LIG_SH2_PTP2 | 242 | 245 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.463 |
LIG_SH3_1 | 228 | 234 | PF00018 | 0.378 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.419 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.379 |
LIG_Sin3_3 | 418 | 425 | PF02671 | 0.387 |
LIG_SUMO_SIM_anti_2 | 126 | 132 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 144 | 150 | PF11976 | 0.234 |
LIG_SUMO_SIM_anti_2 | 450 | 456 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 147 | 154 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 207 | 213 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 450 | 456 | PF11976 | 0.367 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.347 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.425 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.440 |
LIG_UBA3_1 | 392 | 398 | PF00899 | 0.341 |
LIG_UBA3_1 | 56 | 62 | PF00899 | 0.623 |
MOD_CDK_SPxK_1 | 36 | 42 | PF00069 | 0.584 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.451 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.304 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.659 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.424 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.458 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.499 |
MOD_Cter_Amidation | 214 | 217 | PF01082 | 0.469 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.552 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.526 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.425 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.383 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.446 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.475 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.327 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.497 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.456 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.465 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.560 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.570 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.487 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.391 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.425 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.495 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.555 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.466 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.620 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.523 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.537 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.505 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.378 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.476 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.545 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.543 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.402 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.496 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.442 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.522 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.538 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.608 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.568 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_1 | 416 | 421 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_1 | 450 | 455 | PF01217 | 0.411 |
TRG_DiLeu_LyEn_5 | 260 | 265 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.336 |
TRG_NLS_MonoExtN_4 | 395 | 401 | PF00514 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBX3 | Leptomonas seymouri | 52% | 100% |
A0A1X0NIQ1 | Trypanosomatidae | 27% | 100% |
A0A3R7MWR0 | Trypanosoma rangeli | 29% | 98% |
A0A3S7WY18 | Leishmania donovani | 93% | 100% |
A4HD63 | Leishmania braziliensis | 80% | 100% |
A4I0M8 | Leishmania infantum | 93% | 100% |
D0A6X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 99% |
E9AWJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BRC9 | Trypanosoma cruzi | 28% | 99% |