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: 20 |
NetGPI | no | yes: 0, no: 20 |
Related structures:
AlphaFold database: Q4QBB7
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.342 |
CLV_Separin_Metazoa | 4 | 8 | PF03568 | 0.476 |
DEG_APCC_DBOX_1 | 206 | 214 | PF00400 | 0.354 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.601 |
DEG_SCF_FBW7_1 | 115 | 122 | PF00400 | 0.202 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.492 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.643 |
DEG_SPOP_SBC_1 | 457 | 461 | PF00917 | 0.730 |
DOC_CYCLIN_yClb1_LxF_4 | 136 | 141 | PF00134 | 0.320 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 250 | 259 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.386 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.398 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.512 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.332 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 224 | 231 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.259 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.426 |
LIG_Clathr_ClatBox_1 | 139 | 143 | PF01394 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 200 | 208 | PF00928 | 0.347 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.436 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.427 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.600 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.377 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.483 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.463 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.631 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 214 | 218 | PF02991 | 0.440 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 89 | 96 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.322 |
LIG_MYND_1 | 190 | 194 | PF01753 | 0.437 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.428 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.331 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.349 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 86 | 92 | PF11976 | 0.391 |
LIG_TYR_ITIM | 90 | 95 | PF00017 | 0.334 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.504 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.339 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.384 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.474 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.369 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.775 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.723 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.642 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.682 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.325 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.446 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.467 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.560 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.434 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.308 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.409 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.368 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.402 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.449 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.396 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.455 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.541 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.358 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.462 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.477 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.516 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.462 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.371 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.261 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.458 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.447 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.504 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.440 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.369 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.427 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.551 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.511 |
MOD_SUMO_rev_2 | 52 | 59 | PF00179 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.313 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P740 | Leptomonas seymouri | 61% | 100% |
A0A0N1I5Z7 | Leptomonas seymouri | 31% | 100% |
A0A0N1I7E8 | Leptomonas seymouri | 34% | 100% |
A0A1X0NX10 | Trypanosomatidae | 31% | 100% |
A0A1X0NX22 | Trypanosomatidae | 37% | 100% |
A0A1X0NXP4 | Trypanosomatidae | 28% | 100% |
A0A3Q8IM07 | Leishmania donovani | 31% | 100% |
A0A3S7WXP2 | Leishmania donovani | 93% | 100% |
A0A3S7WXT7 | Leishmania donovani | 31% | 100% |
A4HCS3 | Leishmania braziliensis | 77% | 100% |
A4I097 | Leishmania infantum | 93% | 100% |
A4I0B8 | Leishmania infantum | 31% | 100% |
E9AH12 | Leishmania infantum | 31% | 100% |
E9AW61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AW62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AW82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q4QBB6 | Leishmania major | 30% | 81% |
Q9U0V7 | Leishmania major | 32% | 100% |
V5BH08 | Trypanosoma cruzi | 35% | 100% |