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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0005689 | U12-type spliceosomal complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 4 |
GO:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
Related structures:
AlphaFold database: Q4QCI3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 43 | 47 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 41 | 47 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.676 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.766 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.658 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.782 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.808 |
DOC_PP2B_PxIxI_1 | 155 | 161 | PF00149 | 0.622 |
DOC_PP2B_PxIxI_1 | 188 | 194 | PF00149 | 0.625 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.799 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.698 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 217 | 227 | PF00244 | 0.805 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.551 |
LIG_CaM_NSCaTE_8 | 90 | 97 | PF13499 | 0.556 |
LIG_EVH1_1 | 169 | 173 | PF00568 | 0.780 |
LIG_EVH1_1 | 175 | 179 | PF00568 | 0.697 |
LIG_EVH1_2 | 171 | 175 | PF00568 | 0.786 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.731 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.662 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.625 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.574 |
LIG_LIR_Gen_1 | 105 | 113 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 77 | 83 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.517 |
LIG_SH2_CRK | 107 | 111 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 107 | 111 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.517 |
LIG_SH3_1 | 168 | 174 | PF00018 | 0.712 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.727 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.602 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.717 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.766 |
MOD_CDK_SPxxK_3 | 49 | 56 | PF00069 | 0.593 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.790 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.676 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.792 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.761 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.607 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.614 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.716 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.692 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.711 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.721 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.410 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.376 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.376 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.679 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.378 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.816 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.502 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.429 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.430 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.699 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.648 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.737 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.529 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.593 |
MOD_SUMO_rev_2 | 35 | 42 | PF00179 | 0.652 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.569 |
TRG_NES_CRM1_1 | 108 | 120 | PF08389 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0S9 | Leptomonas seymouri | 67% | 100% |
A0A3Q8IA85 | Leishmania donovani | 91% | 97% |
A4HBN0 | Leishmania braziliensis | 79% | 97% |
A4HZ31 | Leishmania infantum | 91% | 97% |
D0A1N1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AUZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |