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: A0A3Q8IG12
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.437 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.357 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.370 |
DEG_SCF_FBW7_1 | 265 | 271 | PF00400 | 0.479 |
DOC_ANK_TNKS_1 | 307 | 314 | PF00023 | 0.392 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.481 |
DOC_MAPK_gen_1 | 101 | 110 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 101 | 110 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 350 | 359 | PF00069 | 0.389 |
DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.366 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.315 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.418 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.546 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.474 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.336 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.414 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.409 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.362 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.545 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.516 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.420 |
LIG_HP1_1 | 42 | 46 | PF01393 | 0.436 |
LIG_LIR_Apic_2 | 326 | 332 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 373 | 384 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.306 |
LIG_Pex14_2 | 325 | 329 | PF04695 | 0.381 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.379 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.502 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.637 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.445 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 104 | 112 | PF11976 | 0.373 |
LIG_TYR_ITIM | 374 | 379 | PF00017 | 0.347 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.496 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.541 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.582 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.340 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.385 |
MOD_CMANNOS | 362 | 365 | PF00535 | 0.331 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.485 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.636 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.515 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.435 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.437 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.380 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.362 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.416 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.460 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.511 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.466 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.431 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.482 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.579 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.413 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.674 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.375 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.335 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.444 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.532 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.346 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.532 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.406 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.562 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.416 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.378 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.510 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.403 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.454 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.346 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M8 | Leptomonas seymouri | 44% | 100% |
A4HK55 | Leishmania braziliensis | 73% | 100% |
A4I7P1 | Leishmania infantum | 99% | 100% |
E9B2J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q5K8 | Leishmania major | 88% | 100% |