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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q8A6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.350 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.536 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.431 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.476 |
DEG_MDM2_SWIB_1 | 275 | 283 | PF02201 | 0.450 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.461 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.613 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.397 |
DOC_CYCLIN_RxL_1 | 242 | 250 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.280 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 353 | 360 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.259 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.380 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.279 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.326 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 245 | 250 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 87 | 91 | PF00244 | 0.491 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.482 |
LIG_BIR_III_2 | 122 | 126 | PF00653 | 0.573 |
LIG_BIR_III_2 | 171 | 175 | PF00653 | 0.454 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.469 |
LIG_CtBP_PxDLS_1 | 55 | 59 | PF00389 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 277 | 281 | PF00928 | 0.448 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.386 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.383 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.456 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.375 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.447 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.495 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.452 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.768 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.477 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.183 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.405 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.443 |
LIG_SH2_GRB2like | 74 | 77 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.395 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.530 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.646 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.418 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.487 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.428 |
LIG_SH3_CIN85_PxpxPR_1 | 240 | 245 | PF14604 | 0.334 |
LIG_SUMO_SIM_anti_2 | 25 | 40 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 245 | 250 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 414 | 419 | PF11976 | 0.436 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.595 |
LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.505 |
LIG_WRC_WIRS_1 | 272 | 277 | PF05994 | 0.466 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.355 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.567 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.491 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.329 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.477 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.617 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.481 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.472 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.644 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.760 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.523 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.603 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.573 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.634 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.564 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.434 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.407 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.620 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.560 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.515 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.418 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.354 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.395 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.452 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.558 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.557 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.545 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.420 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.539 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.467 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.390 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.432 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.499 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.410 |
MOD_PKA_1 | 157 | 163 | PF00069 | 0.419 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.467 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.578 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.439 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.327 |
MOD_Plk_2-3 | 271 | 277 | PF00069 | 0.358 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.521 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.467 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.418 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.513 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.403 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.482 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.378 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.536 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.398 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.481 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.356 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.637 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.519 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.307 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.498 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.490 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.322 |
TRG_DiLeu_BaEn_1 | 395 | 400 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P824 | Leptomonas seymouri | 53% | 100% |
A0A1X0NSF3 | Trypanosomatidae | 35% | 100% |
A0A3R7MSX4 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X1L8 | Leishmania donovani | 94% | 100% |
A4HGL2 | Leishmania braziliensis | 84% | 100% |
A4I3N8 | Leishmania infantum | 95% | 100% |
D0A8C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AZX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5AVA5 | Trypanosoma cruzi | 38% | 100% |