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: Q9NEE1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.570 |
CLV_PCSK_FUR_1 | 114 | 118 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.516 |
CLV_Separin_Metazoa | 130 | 134 | PF03568 | 0.444 |
DEG_SCF_TRCP1_1 | 137 | 143 | PF00400 | 0.518 |
DEG_SPOP_SBC_1 | 148 | 152 | PF00917 | 0.649 |
DOC_CDC14_PxL_1 | 47 | 55 | PF14671 | 0.541 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.551 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.676 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.565 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 42 | 48 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 40 | 56 | PF00022 | 0.518 |
LIG_APCC_ABBAyCdc20_2 | 95 | 101 | PF00400 | 0.520 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_CaM_IQ_9 | 106 | 122 | PF13499 | 0.535 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.548 |
LIG_MYND_1 | 19 | 23 | PF01753 | 0.556 |
LIG_PCNA_yPIPBox_3 | 120 | 132 | PF02747 | 0.434 |
LIG_PDZ_Class_3 | 163 | 168 | PF00595 | 0.654 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.480 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.631 |
LIG_TRAF2_1 | 22 | 25 | PF00917 | 0.545 |
MOD_CDC14_SPxK_1 | 156 | 159 | PF00782 | 0.540 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.541 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.551 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.761 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.635 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.511 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.790 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.573 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.627 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.691 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.642 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.708 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.643 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.600 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.521 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.698 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.670 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.477 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.620 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.587 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.502 |
MOD_PK_1 | 105 | 111 | PF00069 | 0.529 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.618 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.578 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.570 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.600 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.547 |
MOD_SUMO_for_1 | 104 | 107 | PF00179 | 0.424 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.571 |
TRG_NLS_Bipartite_1 | 95 | 117 | PF00514 | 0.486 |
TRG_NLS_MonoExtC_3 | 111 | 116 | PF00514 | 0.500 |
TRG_NLS_MonoExtC_3 | 119 | 124 | PF00514 | 0.495 |
TRG_NLS_MonoExtN_4 | 112 | 117 | PF00514 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WNR8 | Leishmania donovani | 91% | 100% |
A4H443 | Leishmania braziliensis | 85% | 100% |
A4HS56 | Leishmania infantum | 91% | 100% |
C9ZY53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AK43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |