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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6F3
Term | Name | Level | Count |
---|---|---|---|
GO:0019216 | regulation of lipid metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.261 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.372 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.411 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.367 |
DOC_CYCLIN_RxL_1 | 156 | 164 | PF00134 | 0.411 |
DOC_PP4_FxxP_1 | 214 | 217 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.472 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.411 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 28 | 35 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.357 |
LIG_Actin_WH2_2 | 285 | 301 | PF00022 | 0.728 |
LIG_APCC_ABBA_1 | 215 | 220 | PF00400 | 0.411 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.412 |
LIG_Clathr_ClatBox_1 | 243 | 247 | PF01394 | 0.411 |
LIG_DLG_GKlike_1 | 157 | 165 | PF00625 | 0.411 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.261 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.372 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.411 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.643 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.482 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.626 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.639 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.411 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.411 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.411 |
LIG_LIR_LC3C_4 | 242 | 246 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.456 |
LIG_NRBOX | 239 | 245 | PF00104 | 0.411 |
LIG_PCNA_yPIPBox_3 | 383 | 391 | PF02747 | 0.560 |
LIG_Pex14_2 | 210 | 214 | PF04695 | 0.411 |
LIG_Pex14_2 | 7 | 11 | PF04695 | 0.411 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.411 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.789 |
LIG_SH2_GRB2like | 279 | 282 | PF00017 | 0.382 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.754 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.374 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.411 |
LIG_SH3_1 | 363 | 369 | PF00018 | 0.678 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.411 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.369 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.725 |
LIG_SUMO_SIM_anti_2 | 242 | 247 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 241 | 247 | PF11976 | 0.411 |
LIG_SxIP_EBH_1 | 148 | 159 | PF03271 | 0.261 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.411 |
LIG_WW_3 | 364 | 368 | PF00397 | 0.678 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.511 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.462 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.411 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.261 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.415 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.651 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.290 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.411 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.360 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.493 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.250 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.187 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.513 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.513 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.572 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.706 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.378 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.408 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.405 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.290 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.378 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.257 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.411 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.513 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.384 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.529 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.543 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.183 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.435 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.683 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.411 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.429 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.411 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.720 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.433 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.676 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.411 |
MOD_NEK2_2 | 179 | 184 | PF00069 | 0.353 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.261 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.261 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.443 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.411 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.468 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.703 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.393 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.384 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.415 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.617 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.431 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.400 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.411 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.411 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.411 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.428 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.514 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.580 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.601 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.499 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.261 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.261 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2X1 | Leptomonas seymouri | 56% | 93% |
A0A3Q8I8X5 | Leishmania donovani | 74% | 100% |
A4HUU7 | Leishmania infantum | 74% | 100% |
E9ANI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QH44 | Leishmania major | 73% | 98% |