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: A4HK55
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.420 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.505 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.373 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.387 |
DEG_COP1_1 | 232 | 242 | PF00400 | 0.516 |
DEG_SCF_FBW7_1 | 265 | 271 | PF00400 | 0.501 |
DEG_SCF_FBW7_1 | 380 | 387 | PF00400 | 0.287 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.579 |
DOC_MAPK_DCC_7 | 370 | 379 | PF00069 | 0.263 |
DOC_MAPK_MEF2A_6 | 101 | 110 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 350 | 359 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 370 | 379 | PF00069 | 0.263 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.288 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.403 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.278 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.481 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.573 |
LIG_deltaCOP1_diTrp_1 | 364 | 368 | PF00928 | 0.336 |
LIG_EH_1 | 322 | 326 | PF12763 | 0.393 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.527 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.409 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.335 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.326 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.501 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.408 |
LIG_HP1_1 | 375 | 379 | PF01393 | 0.237 |
LIG_HP1_1 | 42 | 46 | PF01393 | 0.459 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.469 |
LIG_LYPXL_SIV_4 | 303 | 311 | PF13949 | 0.346 |
LIG_Pex14_2 | 325 | 329 | PF04695 | 0.426 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.359 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.399 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.451 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.688 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.500 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.600 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.445 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.287 |
MOD_CDC14_SPxK_1 | 155 | 158 | PF00782 | 0.511 |
MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.534 |
MOD_CDK_SPK_2 | 152 | 157 | PF00069 | 0.513 |
MOD_CDK_SPK_2 | 96 | 101 | PF00069 | 0.489 |
MOD_CDK_SPxK_1 | 152 | 158 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.479 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.570 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.570 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.527 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.327 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.420 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.644 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.359 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.536 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.421 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.297 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.337 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.433 |
MOD_CMANNOS | 362 | 365 | PF00535 | 0.333 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.361 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.502 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.581 |
MOD_GlcNHglycan | 247 | 252 | PF01048 | 0.652 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.375 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.456 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.402 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.428 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.480 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.439 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.596 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.477 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.584 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.287 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.346 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.503 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.510 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.439 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.442 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.301 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.366 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.522 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.553 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.359 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.435 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.291 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.491 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.416 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.479 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.502 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.623 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.291 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.554 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M8 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IG12 | Leishmania donovani | 73% | 100% |
A4I7P1 | Leishmania infantum | 73% | 100% |
E9B2J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4Q5K8 | Leishmania major | 73% | 100% |