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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q8T3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.696 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.483 |
DOC_MAPK_gen_1 | 94 | 103 | PF00069 | 0.463 |
DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.494 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.704 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.685 |
DOC_USP7_UBL2_3 | 78 | 82 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 45 | 54 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 102 | 120 | PF00022 | 0.578 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.494 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.545 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.587 |
LIG_SH2_GRB2like | 91 | 94 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.604 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.694 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.702 |
LIG_SUMO_SIM_par_1 | 60 | 67 | PF11976 | 0.377 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.449 |
LIG_UBA3_1 | 72 | 79 | PF00899 | 0.538 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.689 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.624 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.445 |
MOD_Cter_Amidation | 146 | 149 | PF01082 | 0.781 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.502 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.589 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.646 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.663 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.572 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.542 |
MOD_PKA_1 | 78 | 84 | PF00069 | 0.432 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.634 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.680 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.596 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.444 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.620 |
MOD_SUMO_rev_2 | 49 | 59 | PF00179 | 0.614 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.647 |
TRG_DiLeu_BaEn_4 | 30 | 36 | PF01217 | 0.483 |
TRG_DiLeu_LyEn_5 | 49 | 54 | PF01217 | 0.536 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.533 |
TRG_ER_diLys_1 | 148 | 151 | PF00400 | 0.700 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC7 | Leptomonas seymouri | 75% | 100% |
A0A0S4JH37 | Bodo saltans | 37% | 100% |
A0A1X0NEM8 | Trypanosomatidae | 51% | 100% |
A0A3R7R8R4 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X093 | Leishmania donovani | 96% | 100% |
A4HFA2 | Leishmania braziliensis | 83% | 100% |
C9ZX03 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
E9AYN9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |