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: A4HST2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.709 |
CLV_PCSK_FUR_1 | 154 | 158 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.552 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.693 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.795 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.759 |
DOC_MAPK_gen_1 | 179 | 186 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.646 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.624 |
LIG_APCC_ABBA_1 | 18 | 23 | PF00400 | 0.537 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.532 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.579 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.599 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.567 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.796 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.719 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.580 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.630 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.554 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.613 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.740 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.715 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.513 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.794 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.766 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.780 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.468 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.532 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.703 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.718 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.689 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.492 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.689 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.701 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.686 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.725 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.672 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.657 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.630 |
MOD_SUMO_rev_2 | 172 | 181 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 55 | 60 | PF01217 | 0.569 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II80 | Leptomonas seymouri | 53% | 92% |
A0A3S5H5Q2 | Leishmania donovani | 100% | 100% |
A4H4K6 | Leishmania braziliensis | 80% | 100% |
E9AKR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QJ38 | Leishmania major | 96% | 100% |