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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QET6
Term | Name | Level | Count |
---|---|---|---|
GO:0006790 | sulfur compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 11 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0097428 | protein maturation by iron-sulfur cluster transfer | 5 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0051536 | iron-sulfur cluster binding | 3 | 11 |
GO:0051537 | 2 iron, 2 sulfur cluster binding | 4 | 2 |
GO:0051540 | metal cluster binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.272 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.320 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.595 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.704 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.484 |
DOC_CYCLIN_RxL_1 | 14 | 23 | PF00134 | 0.614 |
DOC_CYCLIN_RxL_1 | 153 | 163 | PF00134 | 0.510 |
DOC_PP1_RVXF_1 | 133 | 140 | PF00149 | 0.533 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.573 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.744 |
DOC_USP7_UBL2_3 | 264 | 268 | PF12436 | 0.543 |
DOC_USP7_UBL2_3 | 63 | 67 | PF12436 | 0.613 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.713 |
LIG_BIR_III_2 | 120 | 124 | PF00653 | 0.651 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.612 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.648 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.504 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.458 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.458 |
LIG_LIR_Apic_2 | 266 | 270 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 77 | 81 | PF02991 | 0.641 |
LIG_LIR_LC3C_4 | 228 | 232 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.406 |
LIG_SH2_SRC | 248 | 251 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.458 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.523 |
LIG_SxIP_EBH_1 | 67 | 79 | PF03271 | 0.624 |
LIG_TRFH_1 | 145 | 149 | PF08558 | 0.377 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.525 |
MOD_CDK_SPxxK_3 | 127 | 134 | PF00069 | 0.490 |
MOD_CDK_SPxxK_3 | 215 | 222 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 69 | 76 | PF00069 | 0.682 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.586 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.396 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.453 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.673 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.786 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.677 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.541 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.532 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.550 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.762 |
MOD_DYRK1A_RPxSP_1 | 127 | 131 | PF00069 | 0.478 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.566 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.222 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.280 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.303 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.603 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.722 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.576 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.515 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.506 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.630 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.525 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.423 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.714 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.547 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.775 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.631 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.696 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.755 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.685 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.737 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.573 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.730 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.677 |
MOD_PKB_1 | 192 | 200 | PF00069 | 0.472 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.604 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.532 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.493 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.374 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.629 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.548 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.716 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.674 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6U6 | Leptomonas seymouri | 65% | 100% |
A0A1X0NZ22 | Trypanosomatidae | 59% | 100% |
A0A3Q8IAJ0 | Leishmania donovani | 93% | 100% |
A0A422NDJ9 | Trypanosoma rangeli | 50% | 100% |
A4H8K7 | Leishmania braziliensis | 76% | 100% |
A4HWY0 | Leishmania infantum | 93% | 100% |
C9ZW24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AQP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BHL1 | Trypanosoma cruzi | 49% | 91% |