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: Q4Q5K8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.476 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.483 |
DEG_SCF_FBW7_1 | 265 | 271 | PF00400 | 0.618 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.532 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.618 |
DOC_MAPK_MEF2A_6 | 351 | 358 | PF00069 | 0.459 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.478 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.532 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.702 |
LIG_CaM_IQ_9 | 249 | 265 | PF13499 | 0.408 |
LIG_eIF4E_1 | 160 | 166 | PF01652 | 0.548 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.513 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.551 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.439 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.438 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.616 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.596 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.554 |
LIG_HP1_1 | 42 | 46 | PF01393 | 0.586 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.377 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.459 |
LIG_Pex14_2 | 324 | 328 | PF04695 | 0.563 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.477 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 375 | 378 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 54 | 57 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.238 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.612 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.774 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.581 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.619 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.571 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.567 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.376 |
LIG_TYR_ITIM | 373 | 378 | PF00017 | 0.474 |
LIG_WW_3 | 310 | 314 | PF00397 | 0.524 |
MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.579 |
MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.527 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.617 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.619 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.613 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.435 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.497 |
MOD_CMANNOS | 361 | 364 | PF00535 | 0.455 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.392 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.690 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.652 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.586 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.530 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.464 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.467 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.534 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.555 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.550 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.599 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.521 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.699 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.504 |
MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.544 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.741 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.558 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.537 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.447 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.584 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.443 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.628 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.538 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.669 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.559 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.541 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.584 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.646 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.531 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M8 | Leptomonas seymouri | 44% | 99% |
A0A3Q8IG12 | Leishmania donovani | 88% | 100% |
A4HK55 | Leishmania braziliensis | 73% | 100% |
A4I7P1 | Leishmania infantum | 89% | 100% |
E9B2J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |