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: A0A3S7X7D6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.577 |
CLV_MEL_PAP_1 | 194 | 200 | PF00089 | 0.416 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.673 |
CLV_PCSK_FUR_1 | 285 | 289 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.374 |
CLV_Separin_Metazoa | 366 | 370 | PF03568 | 0.405 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.447 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.622 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.527 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.446 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 321 | 328 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 395 | 402 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 411 | 418 | PF00244 | 0.417 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.423 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.445 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.457 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.539 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.379 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.500 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.558 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.301 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.568 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.513 |
LIG_GBD_Chelix_1 | 132 | 140 | PF00786 | 0.410 |
LIG_HP1_1 | 196 | 200 | PF01393 | 0.429 |
LIG_LIR_Apic_2 | 12 | 17 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 181 | 190 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.604 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.601 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.677 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.464 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.542 |
LIG_SH3_1 | 168 | 174 | PF00018 | 0.583 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.582 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.623 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.369 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.667 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.610 |
LIG_SUMO_SIM_anti_2 | 249 | 255 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 156 | 161 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 352 | 359 | PF11976 | 0.399 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.584 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.557 |
MOD_CDK_SPxK_1 | 67 | 73 | PF00069 | 0.595 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.530 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.608 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.543 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.487 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.586 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.614 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.552 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.515 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.475 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.714 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.518 |
MOD_GlcNHglycan | 50 | 54 | PF01048 | 0.736 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.646 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.618 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.508 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.584 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.422 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.524 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.470 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.564 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.360 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.607 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.481 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.482 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.525 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.492 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.580 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.382 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.415 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.387 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.558 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.368 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.421 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.528 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.442 |
MOD_OFUCOSY | 35 | 40 | PF10250 | 0.480 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.370 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.361 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.421 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.488 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.388 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.443 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.593 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.554 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.545 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.633 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.404 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.538 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.513 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.590 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.622 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.564 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.592 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.768 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.515 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 274 | 283 | PF00179 | 0.601 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 198 | 203 | PF01217 | 0.440 |
TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.402 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW8 | Leptomonas seymouri | 39% | 72% |
A4HAF6 | Leishmania braziliensis | 70% | 98% |
A4I9L2 | Leishmania infantum | 99% | 100% |
E9B4L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3G6 | Leishmania major | 91% | 100% |