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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HNN2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.575 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.585 |
CLV_PCSK_PC7_1 | 54 | 60 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.411 |
DEG_COP1_1 | 4 | 16 | PF00400 | 0.512 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.585 |
DOC_CYCLIN_RxL_1 | 183 | 196 | PF00134 | 0.407 |
DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.324 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.556 |
DOC_USP7_MATH_2 | 70 | 76 | PF00917 | 0.432 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.351 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.419 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 152 | 169 | PF00022 | 0.436 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.408 |
LIG_eIF4E_1 | 104 | 110 | PF01652 | 0.419 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.420 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.379 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.539 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.559 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.483 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.419 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.477 |
LIG_MYND_1 | 94 | 98 | PF01753 | 0.414 |
LIG_NRP_CendR_1 | 222 | 224 | PF00754 | 0.520 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.333 |
LIG_SH3_2 | 64 | 69 | PF14604 | 0.511 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.622 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 105 | 112 | PF11976 | 0.426 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.329 |
MOD_CDC14_SPxK_1 | 66 | 69 | PF00782 | 0.536 |
MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.342 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.650 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.459 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.460 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.461 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.696 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.451 |
MOD_DYRK1A_RPxSP_1 | 63 | 67 | PF00069 | 0.736 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.547 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.566 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.342 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.564 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.466 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.524 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.539 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.546 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.506 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.459 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.390 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.487 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.577 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.518 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.533 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.669 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.481 |
MOD_PKB_1 | 57 | 65 | PF00069 | 0.493 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.337 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.451 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.529 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.476 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.486 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.649 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 153 | 157 | PF00179 | 0.351 |
MOD_SUMO_rev_2 | 171 | 176 | PF00179 | 0.355 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.311 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5U6 | Leptomonas seymouri | 61% | 98% |
A0A1X0P8P1 | Trypanosomatidae | 38% | 97% |
A0A3Q8IQF0 | Leishmania donovani | 82% | 100% |
A4ICW3 | Leishmania infantum | 82% | 100% |
D0A2I6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9ASE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q254 | Leishmania major | 80% | 100% |