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: E9ART9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.758 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.512 |
DEG_SCF_FBW7_1 | 260 | 266 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.440 |
DEG_SPOP_SBC_1 | 364 | 368 | PF00917 | 0.632 |
DOC_CDC14_PxL_1 | 210 | 218 | PF14671 | 0.612 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.362 |
DOC_CKS1_1 | 260 | 265 | PF01111 | 0.535 |
DOC_CYCLIN_RxL_1 | 248 | 255 | PF00134 | 0.665 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.457 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.597 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 44 | 53 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 330 | 347 | PF00022 | 0.431 |
LIG_Actin_WH2_2 | 403 | 420 | PF00022 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.787 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.710 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.710 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.488 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.363 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.595 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.551 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.486 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.678 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.509 |
LIG_LYPXL_yS_3 | 213 | 216 | PF13949 | 0.599 |
LIG_NRBOX | 182 | 188 | PF00104 | 0.561 |
LIG_PDZ_Class_2 | 417 | 422 | PF00595 | 0.679 |
LIG_Pex14_1 | 206 | 210 | PF04695 | 0.607 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.507 |
LIG_REV1ctd_RIR_1 | 50 | 58 | PF16727 | 0.450 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.573 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.294 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.444 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.661 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.307 |
MOD_CDC14_SPxK_1 | 247 | 250 | PF00782 | 0.672 |
MOD_CDC14_SPxK_1 | 255 | 258 | PF00782 | 0.684 |
MOD_CDK_SPxK_1 | 244 | 250 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 252 | 258 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 244 | 251 | PF00069 | 0.742 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.592 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.744 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.546 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.587 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.678 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.512 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.619 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.538 |
MOD_GlcNHglycan | 235 | 239 | PF01048 | 0.485 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.766 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.669 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.633 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.632 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.468 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.660 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.638 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.505 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.527 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.766 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.380 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.690 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.480 |
MOD_LATS_1 | 142 | 148 | PF00433 | 0.549 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.368 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.399 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.501 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.468 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.508 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.541 |
MOD_NEK2_2 | 35 | 40 | PF00069 | 0.443 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.554 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.491 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.393 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.671 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.524 |
MOD_PKB_1 | 298 | 306 | PF00069 | 0.633 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.709 |
MOD_Plk_2-3 | 16 | 22 | PF00069 | 0.600 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.436 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.474 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.529 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.484 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.415 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.444 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.548 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.355 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.624 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.579 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 135 | 138 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 386 | 395 | PF00179 | 0.663 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZP2 | Leptomonas seymouri | 45% | 100% |
A0A3S7WV66 | Leishmania donovani | 86% | 100% |
A4H9Q7 | Leishmania braziliensis | 68% | 100% |
A4HY26 | Leishmania infantum | 86% | 100% |
Q4QDN4 | Leishmania major | 85% | 99% |