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 |
Related structures:
AlphaFold database: A4HJ54
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009306 | protein secretion | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0030254 | protein secretion by the type III secretion system | 4 | 10 |
GO:0032940 | secretion by cell | 3 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0035592 | establishment of protein localization to extracellular region | 4 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046903 | secretion | 4 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0055085 | transmembrane transport | 2 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071692 | protein localization to extracellular region | 5 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071806 | protein transmembrane transport | 3 | 10 |
GO:0140352 | export from cell | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 10 | 14 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.611 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 239 | 247 | PF00400 | 0.479 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.526 |
DEG_SPOP_SBC_1 | 272 | 276 | PF00917 | 0.542 |
DOC_MAPK_gen_1 | 15 | 21 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 189 | 196 | PF00069 | 0.542 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.688 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 280 | 287 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.433 |
LIG_APCC_ABBA_1 | 192 | 197 | PF00400 | 0.398 |
LIG_APCC_ABBA_1 | 291 | 296 | PF00400 | 0.519 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_2 | 192 | 198 | PF00533 | 0.540 |
LIG_CaM_IQ_9 | 114 | 130 | PF13499 | 0.399 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.479 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.461 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.461 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.504 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.470 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.721 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.811 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.542 |
LIG_Integrin_RGD_1 | 22 | 24 | PF01839 | 0.462 |
LIG_Integrin_RGD_TGFB_3 | 22 | 28 | PF01839 | 0.431 |
LIG_LIR_Apic_2 | 39 | 43 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.521 |
LIG_MLH1_MIPbox_1 | 192 | 196 | PF16413 | 0.398 |
LIG_NRBOX | 242 | 248 | PF00104 | 0.420 |
LIG_PTAP_UEV_1 | 88 | 93 | PF05743 | 0.539 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.542 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.498 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 102 | 105 | PF00017 | 0.741 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.400 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.713 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 269 | 276 | PF11976 | 0.462 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.540 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.425 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.540 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.615 |
MOD_Cter_Amidation | 13 | 16 | PF01082 | 0.513 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.629 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.218 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.490 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.667 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.469 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.479 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.458 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.553 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.261 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.489 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.479 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.414 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.458 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.469 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.474 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.576 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.539 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.616 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.461 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.461 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.464 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.496 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.479 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.479 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_1 | 44 | 49 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT22 | Leptomonas seymouri | 54% | 93% |
A0A0S4IPP0 | Bodo saltans | 30% | 67% |
A0A3S7X487 | Leishmania donovani | 74% | 98% |
A4I6G8 | Leishmania infantum | 74% | 98% |
D0A443 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 85% |
E9B1M5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 94% |
Q9BHG3 | Leishmania major | 73% | 100% |
V5BJ53 | Trypanosoma cruzi | 46% | 88% |