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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AUS8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.735 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.625 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.625 |
CLV_PCSK_PC7_1 | 371 | 377 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.640 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.644 |
DEG_SIAH_1 | 326 | 334 | PF03145 | 0.663 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.536 |
DOC_CYCLIN_RxL_1 | 371 | 381 | PF00134 | 0.620 |
DOC_MAPK_gen_1 | 275 | 283 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 383 | 392 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 383 | 392 | PF00069 | 0.574 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 113 | 118 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 81 | 85 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.624 |
LIG_APCC_ABBA_1 | 395 | 400 | PF00400 | 0.600 |
LIG_BIR_III_4 | 356 | 360 | PF00653 | 0.636 |
LIG_Clathr_ClatBox_1 | 408 | 412 | PF01394 | 0.415 |
LIG_DLG_GKlike_1 | 113 | 120 | PF00625 | 0.685 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.574 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.627 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.603 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.515 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.567 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.628 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.461 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.775 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.740 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.571 |
LIG_PCNA_yPIPBox_3 | 383 | 396 | PF02747 | 0.406 |
LIG_Pex14_1 | 179 | 183 | PF04695 | 0.604 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 35 | 39 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 443 | 446 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.606 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 404 | 410 | PF11976 | 0.647 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.703 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.763 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.642 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.778 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.709 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.694 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.581 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.619 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.718 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.460 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.761 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.657 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.741 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.526 |
MOD_GlcNHglycan | 200 | 204 | PF01048 | 0.671 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.759 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.502 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.596 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.746 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.660 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.579 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.597 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.710 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.789 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.670 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.676 |
MOD_LATS_1 | 95 | 101 | PF00433 | 0.721 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.681 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.617 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.701 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.553 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.717 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.460 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.629 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.576 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.586 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.517 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.704 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.618 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.685 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.709 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.666 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.606 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.661 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.684 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.666 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.726 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.565 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.536 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.577 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.740 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.652 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.731 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.718 |
MOD_SUMO_rev_2 | 185 | 191 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 334 | 342 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.609 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.593 |
TRG_NES_CRM1_1 | 386 | 400 | PF08389 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 170 | 175 | PF00026 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 247 | 252 | PF00026 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WW39 | Leishmania donovani | 85% | 100% |
A4HYY2 | Leishmania infantum | 85% | 100% |
E9AIJ6 | Leishmania braziliensis | 66% | 100% |
Q4QCQ5 | Leishmania major | 83% | 100% |