Uncharacterized Protein, Uncharacterized
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S7WXW4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0047710 | bis(5'-adenosyl)-triphosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.531 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.489 |
DEG_COP1_1 | 81 | 91 | PF00400 | 0.567 |
DEG_SCF_FBW7_2 | 169 | 174 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.444 |
DEG_SPOP_SBC_1 | 343 | 347 | PF00917 | 0.451 |
DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.694 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.572 |
DOC_CYCLIN_RxL_1 | 330 | 340 | PF00134 | 0.408 |
DOC_PP1_RVXF_1 | 235 | 241 | PF00149 | 0.405 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.557 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.457 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 178 | 182 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.496 |
LIG_AP2alpha_2 | 90 | 92 | PF02296 | 0.447 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.532 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 233 | 240 | PF00928 | 0.405 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.583 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.668 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.464 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.488 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.450 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.377 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.556 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.608 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.502 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.495 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.638 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.706 |
LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 180 | 185 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.581 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.569 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.511 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.482 |
LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.586 |
LIG_SH3_1 | 316 | 322 | PF00018 | 0.593 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.361 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.472 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.513 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.442 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.603 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.662 |
LIG_SH3_4 | 139 | 146 | PF00018 | 0.468 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.578 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.484 |
LIG_TRFH_1 | 69 | 73 | PF08558 | 0.583 |
LIG_WW_3 | 317 | 321 | PF00397 | 0.529 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.596 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.529 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.668 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.521 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.442 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.737 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.708 |
MOD_GlcNHglycan | 108 | 113 | PF01048 | 0.690 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.470 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.341 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.813 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.427 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.643 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.570 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.425 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.693 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.471 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.592 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.482 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.550 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.325 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.463 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.627 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.477 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.331 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.463 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.342 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.567 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.371 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.640 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.564 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.557 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.569 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.552 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.386 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.644 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.508 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.561 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.526 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.591 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.588 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P352 | Leptomonas seymouri | 57% | 81% |
A0A1X0NWV2 | Trypanosomatidae | 39% | 77% |
A4HCX7 | Leishmania braziliensis | 83% | 100% |
A4I0G0 | Leishmania infantum | 100% | 100% |
C9ZV80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 84% |
E9AWC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QB49 | Leishmania major | 93% | 100% |
V5BJC2 | Trypanosoma cruzi | 45% | 86% |