Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 9 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 2 |
GO:0005741 | mitochondrial outer membrane | 5 | 17 |
GO:0016020 | membrane | 2 | 17 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 2 |
GO:0019867 | outer membrane | 3 | 17 |
GO:0020022 | acidocalcisome | 5 | 2 |
GO:0031090 | organelle membrane | 3 | 17 |
GO:0031966 | mitochondrial membrane | 4 | 17 |
GO:0031968 | organelle outer membrane | 4 | 17 |
GO:0032991 | protein-containing complex | 1 | 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:0046930 | pore complex | 3 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 17 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: E9ACC0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006839 | mitochondrial transport | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0046907 | intracellular transport | 3 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0051641 | cellular localization | 2 | 3 |
GO:0051649 | establishment of localization in cell | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 17 |
GO:0005216 | monoatomic ion channel activity | 4 | 17 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 17 |
GO:0005253 | monoatomic anion channel activity | 5 | 17 |
GO:0008308 | voltage-gated monoatomic anion channel activity | 5 | 17 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 17 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 17 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 17 |
GO:0015267 | channel activity | 4 | 17 |
GO:0015288 | porin activity | 6 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 17 |
GO:0022803 | passive transmembrane transporter activity | 3 | 17 |
GO:0022829 | wide pore channel activity | 5 | 2 |
GO:0022832 | voltage-gated channel activity | 6 | 17 |
GO:0022836 | gated channel activity | 5 | 17 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.543 |
CLV_Separin_Metazoa | 88 | 92 | PF03568 | 0.424 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.537 |
DOC_MAPK_gen_1 | 225 | 234 | PF00069 | 0.545 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.655 |
DOC_USP7_UBL2_3 | 22 | 26 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.221 |
LIG_Actin_WH2_2 | 67 | 84 | PF00022 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.668 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.541 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.528 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.410 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.457 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.438 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.429 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.457 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.476 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.429 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.538 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.499 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.397 |
LIG_Integrin_RGD_1 | 227 | 229 | PF01839 | 0.549 |
LIG_LIR_Apic_2 | 45 | 51 | PF02991 | 0.377 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 23 | 32 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.419 |
LIG_Pex14_1 | 260 | 264 | PF04695 | 0.393 |
LIG_RPA_C_Fungi | 207 | 219 | PF08784 | 0.359 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.549 |
LIG_SH2_CRK | 24 | 28 | PF00017 | 0.494 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 15 | 19 | PF00017 | 0.549 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 99 | 102 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.548 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.541 |
LIG_UBA3_1 | 89 | 94 | PF00899 | 0.455 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.478 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.482 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.499 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.397 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.488 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.565 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.447 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.520 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.508 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.421 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.422 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.646 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.515 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.375 |
MOD_N-GLC_2 | 169 | 171 | PF02516 | 0.520 |
MOD_N-GLC_2 | 211 | 213 | PF02516 | 0.422 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.675 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.511 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.552 |
MOD_NEK2_2 | 246 | 251 | PF00069 | 0.492 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.489 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.492 |
MOD_PK_1 | 131 | 137 | PF00069 | 0.519 |
MOD_PKA_1 | 131 | 137 | PF00069 | 0.378 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.525 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.348 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.401 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.538 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.493 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.536 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.513 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.495 |
MOD_SUMO_rev_2 | 62 | 68 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 88 | 96 | PF00179 | 0.550 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUD3 | Leptomonas seymouri | 68% | 98% |
A0A0N1IIR1 | Leptomonas seymouri | 31% | 100% |
A0A0S4JQ02 | Bodo saltans | 35% | 100% |
A0A1X0NJX9 | Trypanosomatidae | 44% | 100% |
A0A3R7M1M0 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H502 | Leishmania donovani | 31% | 100% |
A0A3S5H503 | Leishmania donovani | 97% | 100% |
A0A422NPQ5 | Trypanosoma rangeli | 45% | 100% |
A4H3D7 | Leishmania braziliensis | 75% | 100% |
A4HRP1 | Leishmania infantum | 31% | 100% |
A4HRP2 | Leishmania infantum | 97% | 100% |
C9ZJ24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACB9 | Leishmania major | 29% | 100% |
E9AJK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AJK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |