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: A4HC74
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.525 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.678 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.516 |
DOC_ANK_TNKS_1 | 391 | 398 | PF00023 | 0.531 |
DOC_CYCLIN_RxL_1 | 425 | 436 | PF00134 | 0.664 |
DOC_MAPK_DCC_7 | 294 | 304 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 267 | 274 | PF00069 | 0.498 |
DOC_MAPK_NFAT4_5 | 267 | 275 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 427 | 434 | PF00149 | 0.677 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.492 |
DOC_USP7_UBL2_3 | 425 | 429 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 403 | 413 | PF00244 | 0.727 |
LIG_BIR_III_2 | 436 | 440 | PF00653 | 0.689 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.569 |
LIG_CtBP_PxDLS_1 | 414 | 418 | PF00389 | 0.535 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.599 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.665 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.528 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.519 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.603 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.611 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.537 |
LIG_LIR_Apic_2 | 99 | 105 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.616 |
LIG_Pex14_1 | 104 | 108 | PF04695 | 0.477 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.492 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.453 |
LIG_SH3_1 | 295 | 301 | PF00018 | 0.506 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.759 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.606 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.615 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.687 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.593 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.557 |
LIG_SUMO_SIM_par_1 | 207 | 215 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 229 | 234 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 300 | 306 | PF11976 | 0.515 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.653 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.519 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.534 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.529 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.509 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.671 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.589 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.513 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.659 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.554 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.786 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.513 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.532 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.667 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.692 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.628 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.609 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.470 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.539 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.624 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.596 |
MOD_GlcNHglycan | 183 | 187 | PF01048 | 0.501 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.660 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.556 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.458 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.513 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.806 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.620 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.528 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.617 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.467 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.642 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.752 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.721 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.519 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.700 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.504 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.538 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.461 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.546 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.544 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.547 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.566 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.472 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.457 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.500 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.533 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.593 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.703 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.536 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.724 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.544 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.742 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.553 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.587 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.675 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.523 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.512 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.467 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.609 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.512 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.669 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.691 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.789 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.503 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.493 |
MOD_SUMO_rev_2 | 177 | 184 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_4 | 265 | 271 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.513 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.489 |
TRG_NLS_MonoExtC_3 | 171 | 177 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 169 | 176 | PF00514 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7A5 | Leishmania donovani | 53% | 100% |
A4HZQ1 | Leishmania infantum | 53% | 100% |
E9AVK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
Q4QBX2 | Leishmania major | 52% | 100% |