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: E9B0B1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.430 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.577 |
DOC_USP7_MATH_2 | 14 | 20 | PF00917 | 0.551 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.611 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.583 |
LIG_BIR_III_4 | 357 | 361 | PF00653 | 0.577 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.356 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.465 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.499 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.418 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.589 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.570 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.514 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.484 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 318 | 328 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 142 | 146 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.511 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.313 |
LIG_RPA_C_Fungi | 46 | 58 | PF08784 | 0.597 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.405 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 293 | 297 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 78 | 82 | PF00017 | 0.455 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.314 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 317 | 320 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 34 | 37 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.517 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.717 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.708 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.595 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.644 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 129 | 136 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 242 | 249 | PF11976 | 0.392 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.434 |
LIG_WRC_WIRS_1 | 321 | 326 | PF05994 | 0.305 |
LIG_WW_3 | 12 | 16 | PF00397 | 0.566 |
MOD_CDC14_SPxK_1 | 12 | 15 | PF00782 | 0.502 |
MOD_CDK_SPxK_1 | 9 | 15 | PF00069 | 0.500 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.513 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.585 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.636 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.584 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.473 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.567 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.477 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.483 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.523 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.505 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.533 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.524 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.619 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.548 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.567 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.591 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.531 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.539 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.603 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.412 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.523 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.542 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.539 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.457 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.466 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.595 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.362 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.377 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.569 |
MOD_Plk_2-3 | 263 | 269 | PF00069 | 0.464 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.384 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.360 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.536 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.489 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.521 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.669 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.628 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 145 | 154 | PF00179 | 0.403 |
TRG_DiLeu_BaEn_1 | 206 | 211 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_2 | 149 | 155 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_2 | 305 | 311 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.647 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5J9 | Leptomonas seymouri | 48% | 100% |
A0A3S7X1Y7 | Leishmania donovani | 86% | 100% |
A4HGZ2 | Leishmania braziliensis | 71% | 100% |
A4I424 | Leishmania infantum | 86% | 100% |
Q4Q7X3 | Leishmania major | 85% | 100% |