A Zn-finger protein with a TM segment on the C-terminus (2 paralogous lineages in Kinetoplastids: A4HSS9_LEIINvs. A4I356_LEIIN). Unlikely to be GPI-anchored due to reverse topology. Weakly similar to NLRC3/NOD3 intracellular immune receptor.
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: 1, no: 12 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 14 |
GO:0042995 | cell projection | 2 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043227 | membrane-bounded organelle | 3 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 14 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 6 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AKR6
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003729 | mRNA binding | 5 | 10 |
GO:0005488 | binding | 1 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043169 | cation binding | 3 | 14 |
GO:0046872 | metal ion binding | 4 | 14 |
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 | 29 | 33 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.444 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.705 |
DEG_SPOP_SBC_1 | 299 | 303 | PF00917 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 314 | 320 | PF00134 | 0.484 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.484 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.490 |
LIG_APCC_ABBA_1 | 80 | 85 | PF00400 | 0.421 |
LIG_APCC_ABBAyCdc20_2 | 19 | 25 | PF00400 | 0.449 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.594 |
LIG_EH_1 | 191 | 195 | PF12763 | 0.390 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.395 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.471 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.407 |
LIG_SH2_NCK_1 | 284 | 288 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 266 | 269 | PF00017 | 0.268 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.319 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.516 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.256 |
LIG_SH3_4 | 7 | 14 | PF00018 | 0.397 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 360 | 365 | PF11976 | 0.387 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.228 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.490 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.376 |
LIG_UBA3_1 | 116 | 121 | PF00899 | 0.350 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.356 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.326 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.618 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.629 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.671 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.401 |
MOD_GlcNHglycan | 133 | 137 | PF01048 | 0.383 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.656 |
MOD_GlcNHglycan | 288 | 292 | PF01048 | 0.650 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.599 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.472 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.584 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.715 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.601 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.408 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.423 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.417 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.383 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.417 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.728 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.572 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.303 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.554 |
MOD_PK_1 | 170 | 176 | PF00069 | 0.401 |
MOD_PKA_1 | 18 | 24 | PF00069 | 0.624 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.648 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.533 |
MOD_PKB_1 | 307 | 315 | PF00069 | 0.650 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.365 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.445 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.453 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.632 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.761 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.683 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.420 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.347 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.457 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.467 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.725 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.619 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.548 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.571 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.283 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.371 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.728 |
MOD_SUMO_rev_2 | 203 | 211 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.465 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.564 |
TRG_NLS_MonoExtC_3 | 229 | 234 | PF00514 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.262 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4T9 | Leptomonas seymouri | 22% | 100% |
A0A1X0NM91 | Trypanosomatidae | 53% | 90% |
A0A3R7KZS1 | Trypanosoma rangeli | 53% | 92% |
A0A3S5H5P9 | Leishmania donovani | 95% | 93% |
A0A3S7X0C2 | Leishmania donovani | 21% | 100% |
A4H4K3 | Leishmania braziliensis | 85% | 100% |
A4HFD8 | Leishmania braziliensis | 22% | 100% |
A4HSS9 | Leishmania infantum | 95% | 93% |
A4I356 | Leishmania infantum | 21% | 100% |
C9ZTD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 95% |
Q4QJ41 | Leishmania major | 94% | 100% |
V5BXP3 | Trypanosoma cruzi | 57% | 92% |