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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.419 |
CLV_PCSK_FUR_1 | 19 | 23 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.553 |
DEG_APCC_KENBOX_2 | 122 | 126 | PF00400 | 0.561 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.585 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.652 |
DOC_PP1_RVXF_1 | 23 | 30 | PF00149 | 0.488 |
DOC_PP1_RVXF_1 | 69 | 76 | PF00149 | 0.401 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 204 | 208 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.294 |
LIG_deltaCOP1_diTrp_1 | 255 | 262 | PF00928 | 0.417 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.441 |
LIG_LIR_Apic_2 | 313 | 317 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 181 | 189 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 238 | 249 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.386 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.328 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.486 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.511 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.359 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.419 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.600 |
LIG_SUMO_SIM_anti_2 | 110 | 116 | PF11976 | 0.498 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.360 |
LIG_UBA3_1 | 111 | 120 | PF00899 | 0.418 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.394 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.486 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.327 |
MOD_CMANNOS | 257 | 260 | PF00535 | 0.412 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.536 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.307 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.441 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.504 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.511 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.546 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.462 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.436 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.580 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.464 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.455 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.328 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.361 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.399 |
MOD_SUMO_rev_2 | 265 | 270 | PF00179 | 0.434 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.439 |
TRG_NES_CRM1_1 | 164 | 176 | PF08389 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F9 | Leptomonas seymouri | 81% | 100% |
A0A0S4J3G5 | Bodo saltans | 46% | 86% |
A0A1X0NHG3 | Trypanosomatidae | 71% | 99% |
A0A3Q8IL95 | Leishmania donovani | 92% | 100% |
A0A3R7N7R7 | Trypanosoma rangeli | 68% | 99% |
A4HZG7 | Leishmania infantum | 92% | 100% |
D0A108 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 99% |
E9AVF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QC22 | Leishmania major | 92% | 100% |
V5BHD8 | Trypanosoma cruzi | 71% | 100% |