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: A0A3S7X5K4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.680 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.673 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.707 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.661 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.735 |
LIG_APCC_ABBA_1 | 34 | 39 | PF00400 | 0.590 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.694 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.716 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.635 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.731 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.638 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.667 |
LIG_NRP_CendR_1 | 150 | 153 | PF00754 | 0.722 |
LIG_PCNA_PIPBox_1 | 121 | 130 | PF02747 | 0.545 |
LIG_Pex14_1 | 28 | 32 | PF04695 | 0.620 |
LIG_PTB_Apo_2 | 126 | 133 | PF02174 | 0.553 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.589 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.634 |
LIG_WRC_WIRS_1 | 124 | 129 | PF05994 | 0.588 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.745 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.683 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.654 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.640 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.618 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.686 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.638 |
MOD_Cter_Amidation | 147 | 150 | PF01082 | 0.607 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.642 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.645 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.647 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.604 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.673 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.626 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.650 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.561 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.514 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.593 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.565 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.674 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.757 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.739 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.723 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.671 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.554 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.639 |
MOD_SUMO_for_1 | 101 | 104 | PF00179 | 0.657 |
TRG_DiLeu_BaEn_2 | 132 | 138 | PF01217 | 0.594 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.722 |
TRG_NLS_MonoExtC_3 | 148 | 153 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 146 | 153 | PF00514 | 0.713 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P974 | Leptomonas seymouri | 51% | 100% |
A0A1X0NT35 | Trypanosomatidae | 32% | 90% |
A0A422NH51 | Trypanosoma rangeli | 29% | 95% |
A4HKG8 | Leishmania braziliensis | 74% | 100% |
A4I7Z5 | Leishmania infantum | 99% | 100% |
D0AA62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
E9B2V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q599 | Leishmania major | 93% | 100% |