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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: A4HCF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.685 |
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.310 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.356 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.436 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.183 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.554 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.395 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.299 |
DOC_MAPK_gen_1 | 266 | 275 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 290 | 298 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.376 |
DOC_MAPK_NFAT4_5 | 63 | 71 | PF00069 | 0.346 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.283 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 116 | 120 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 213 | 217 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 276 | 284 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 63 | 69 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 437 | 452 | PF00022 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.673 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.461 |
LIG_Clathr_ClatBox_1 | 283 | 287 | PF01394 | 0.468 |
LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 200 | 206 | PF00928 | 0.420 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.420 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.366 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.615 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.280 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.428 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.343 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.532 |
LIG_Integrin_RGD_1 | 74 | 76 | PF01839 | 0.432 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.356 |
LIG_LRP6_Inhibitor_1 | 226 | 232 | PF00058 | 0.253 |
LIG_SH2_CRK | 24 | 28 | PF00017 | 0.353 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.159 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.432 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.464 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.307 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.506 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 26 | 32 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 169 | 174 | PF11976 | 0.420 |
LIG_UBA3_1 | 406 | 414 | PF00899 | 0.308 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.413 |
LIG_WW_1 | 21 | 24 | PF00397 | 0.418 |
MOD_CDK_SPK_2 | 116 | 121 | PF00069 | 0.477 |
MOD_CDK_SPxxK_3 | 388 | 395 | PF00069 | 0.325 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.785 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.279 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.438 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.494 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.363 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.627 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.334 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.407 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.384 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.725 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.588 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.504 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.371 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.522 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.724 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.414 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.357 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.345 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.326 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.394 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.491 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.427 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.377 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.537 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.570 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.673 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.641 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.564 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.390 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.407 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.444 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.417 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.388 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.548 |
MOD_NEK2_2 | 148 | 153 | PF00069 | 0.290 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.434 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.580 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.376 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.545 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.311 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.323 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.342 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.458 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.455 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.354 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.462 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.384 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.388 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.384 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.410 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.505 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.543 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.462 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.692 |
MOD_SUMO_for_1 | 98 | 101 | PF00179 | 0.510 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.446 |
TRG_NES_CRM1_1 | 377 | 388 | PF08389 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M2 | Leptomonas seymouri | 65% | 100% |
A0A0N1PFX0 | Leptomonas seymouri | 35% | 100% |
A0A0S4J8Q0 | Bodo saltans | 39% | 100% |
A0A1X0NTE2 | Trypanosomatidae | 39% | 100% |
A0A1X0NX03 | Trypanosomatidae | 24% | 100% |
A0A3Q8IFK3 | Leishmania donovani | 86% | 100% |
A0A3S7WXD8 | Leishmania donovani | 46% | 100% |
A0A422NHR8 | Trypanosoma rangeli | 39% | 100% |
A4HZY3 | Leishmania infantum | 86% | 100% |
A4HZY4 | Leishmania infantum | 46% | 100% |
C9ZSM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AVU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AVU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4QBN4 | Leishmania major | 45% | 100% |
Q4QBN5 | Leishmania major | 85% | 98% |
V5BVW3 | Trypanosoma cruzi | 41% | 100% |