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: A4HKZ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.782 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.802 |
CLV_PCSK_FUR_1 | 368 | 372 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 419 | 421 | PF00082 | 0.812 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.513 |
DEG_MDM2_SWIB_1 | 220 | 228 | PF02201 | 0.693 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.768 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.487 |
DEG_SPOP_SBC_1 | 389 | 393 | PF00917 | 0.624 |
DOC_CDC14_PxL_1 | 190 | 198 | PF14671 | 0.536 |
DOC_CYCLIN_RxL_1 | 74 | 87 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.480 |
DOC_PP1_RVXF_1 | 42 | 49 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.489 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.793 |
LIG_14-3-3_CanoR_1 | 120 | 130 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 388 | 394 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 444 | 449 | PF00244 | 0.707 |
LIG_Actin_WH2_2 | 156 | 174 | PF00022 | 0.684 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.486 |
LIG_CSL_BTD_1 | 47 | 50 | PF09270 | 0.489 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.448 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.517 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.575 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.558 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.771 |
LIG_GBD_Chelix_1 | 206 | 214 | PF00786 | 0.716 |
LIG_GBD_Chelix_1 | 53 | 61 | PF00786 | 0.718 |
LIG_HP1_1 | 435 | 439 | PF01393 | 0.520 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 8 | 14 | PF02991 | 0.549 |
LIG_LIR_LC3C_4 | 433 | 438 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.548 |
LIG_MYND_1 | 278 | 282 | PF01753 | 0.571 |
LIG_Pex14_1 | 213 | 217 | PF04695 | 0.698 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.688 |
LIG_SH2_STAT3 | 299 | 302 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.469 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.711 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.644 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.622 |
LIG_Sin3_3 | 129 | 136 | PF02671 | 0.477 |
LIG_SUMO_SIM_par_1 | 435 | 441 | PF11976 | 0.675 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.544 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.773 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.742 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.603 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.727 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.658 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.586 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.826 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.544 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.504 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.563 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.568 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.637 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.654 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.737 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.799 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.498 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.604 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.681 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.698 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.637 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.566 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.821 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.587 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.695 |
MOD_LATS_1 | 340 | 346 | PF00433 | 0.555 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.695 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.627 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.717 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.554 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.542 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.829 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.457 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.577 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.538 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.461 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.559 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.636 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.407 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.629 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.714 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.559 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.630 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.482 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.616 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.710 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.568 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.747 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.696 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.521 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.688 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.790 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.531 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 443 | 446 | PF00400 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7T2 | Leishmania donovani | 57% | 100% |
A4I8H5 | Leishmania infantum | 57% | 100% |
E9B3D5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
Q4Q4R7 | Leishmania major | 58% | 98% |