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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QEA9
Term | Name | Level | Count |
---|---|---|---|
GO:0044087 | regulation of cellular component biogenesis | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0090069 | regulation of ribosome biogenesis | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.797 |
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.731 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.663 |
CLV_PCSK_FUR_1 | 137 | 141 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.750 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.611 |
CLV_PCSK_PC7_1 | 132 | 138 | PF00082 | 0.788 |
CLV_PCSK_PC7_1 | 156 | 162 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.559 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.672 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.744 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.741 |
DOC_USP7_UBL2_3 | 28 | 32 | PF12436 | 0.414 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.444 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 78 | 87 | PF00244 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.628 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.369 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.677 |
LIG_LIR_Gen_1 | 29 | 38 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.560 |
LIG_SH2_CRK | 68 | 72 | PF00017 | 0.592 |
LIG_SH2_PTP2 | 30 | 33 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.348 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.727 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.645 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.585 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.686 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.544 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.602 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.600 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.656 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.682 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.721 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.560 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.687 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.636 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.784 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.432 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.712 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.628 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.667 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.401 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.665 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.608 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.627 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.644 |
MOD_PKB_1 | 78 | 86 | PF00069 | 0.629 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.579 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.369 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 114 | 123 | PF00179 | 0.765 |
MOD_SUMO_rev_2 | 152 | 162 | PF00179 | 0.764 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.589 |
TRG_NLS_MonoExtC_3 | 135 | 140 | PF00514 | 0.723 |
TRG_NLS_MonoExtC_3 | 159 | 165 | PF00514 | 0.730 |
TRG_NLS_MonoExtC_3 | 75 | 80 | PF00514 | 0.659 |
TRG_NLS_MonoExtN_4 | 73 | 80 | PF00514 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6K7 | Leptomonas seymouri | 53% | 99% |
A0A0S4J7Y3 | Bodo saltans | 35% | 100% |
A0A3S5H710 | Leishmania donovani | 96% | 100% |
A4H945 | Leishmania braziliensis | 75% | 98% |
A4HXF9 | Leishmania infantum | 95% | 100% |
C9ZP33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AR54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5AQX6 | Trypanosoma cruzi | 41% | 78% |