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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q2I9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.506 |
DEG_SCF_FBW7_1 | 318 | 325 | PF00400 | 0.307 |
DOC_CKS1_1 | 11 | 16 | PF01111 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 354 | 360 | PF00134 | 0.257 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.234 |
DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.179 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.278 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 311 | 326 | PF00022 | 0.176 |
LIG_APCC_ABBA_1 | 249 | 254 | PF00400 | 0.387 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.308 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.433 |
LIG_deltaCOP1_diTrp_1 | 179 | 189 | PF00928 | 0.659 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.496 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.375 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.567 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.327 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.298 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.254 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.227 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.401 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.598 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.484 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.422 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.343 |
LIG_MLH1_MIPbox_1 | 53 | 57 | PF16413 | 0.456 |
LIG_PDZ_Class_3 | 403 | 408 | PF00595 | 0.388 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.387 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.191 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.138 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.277 |
LIG_SH3_1 | 200 | 206 | PF00018 | 0.617 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.558 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.725 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.585 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.273 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.387 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.378 |
LIG_SUMO_SIM_par_1 | 247 | 254 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 76 | 82 | PF11976 | 0.319 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.595 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.456 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.434 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.307 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.721 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.412 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.639 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.558 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.613 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.568 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.560 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.494 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.613 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.741 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.417 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.618 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.622 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.580 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.558 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.382 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.431 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.490 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.505 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.381 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.597 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.367 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.399 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.656 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.466 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.263 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.647 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.399 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.614 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.660 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.276 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.238 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.274 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.258 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.482 |
MOD_NEK2_2 | 271 | 276 | PF00069 | 0.485 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.311 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.242 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.626 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.482 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.291 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.613 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.577 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.414 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.544 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.296 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.374 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.735 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.652 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.429 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.179 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.278 |
MOD_SUMO_rev_2 | 192 | 202 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 365 | 372 | PF00179 | 0.304 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYV7 | Leptomonas seymouri | 63% | 100% |
A0A0S4JQH8 | Bodo saltans | 30% | 100% |
A0A1X0PA07 | Trypanosomatidae | 35% | 100% |
A0A3R7N1R1 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X8B9 | Leishmania donovani | 91% | 100% |
A4HB73 | Leishmania braziliensis | 76% | 100% |
A4IAC1 | Leishmania infantum | 91% | 100% |
C9ZLX1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B5E4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P87156 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q5ZID2 | Gallus gallus | 24% | 100% |
Q8C5N5 | Mus musculus | 24% | 100% |
V5DMW4 | Trypanosoma cruzi | 34% | 100% |