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 |
Related structures:
AlphaFold database: A4HCX7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
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 | 0.629 |
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.536 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.630 |
DOC_PP1_RVXF_1 | 331 | 337 | PF00149 | 0.420 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.753 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 178 | 182 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 24 | 31 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.605 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.496 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.711 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.480 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.585 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.449 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.633 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.670 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.600 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.513 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.546 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.732 |
LIG_LIR_Apic_2 | 180 | 185 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.509 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.578 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.661 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.566 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.594 |
LIG_SH2_STAT3 | 194 | 197 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.633 |
LIG_SH3_1 | 316 | 322 | PF00018 | 0.652 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.497 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.366 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.496 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.652 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.573 |
LIG_SH3_4 | 139 | 146 | PF00018 | 0.613 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.747 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.521 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.534 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.587 |
LIG_TRFH_1 | 69 | 73 | PF08558 | 0.732 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.504 |
LIG_UBA3_1 | 169 | 174 | PF00899 | 0.721 |
LIG_WW_3 | 317 | 321 | PF00397 | 0.606 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.551 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.700 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.739 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.575 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.597 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.482 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.734 |
MOD_GlcNHglycan | 108 | 113 | PF01048 | 0.694 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.326 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.349 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.795 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.668 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.567 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.551 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.412 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.594 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.599 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.679 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.362 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.539 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.497 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.529 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.508 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.479 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.653 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.532 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.502 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.541 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.651 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.648 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.562 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.722 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.553 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.717 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.673 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.637 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.652 |
TRG_DiLeu_BaEn_4 | 327 | 333 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 333 | 338 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P352 | Leptomonas seymouri | 56% | 81% |
A0A0S4JIU0 | Bodo saltans | 31% | 92% |
A0A1X0NWV2 | Trypanosomatidae | 38% | 77% |
A0A3S7WXW4 | Leishmania donovani | 83% | 100% |
A4I0G0 | Leishmania infantum | 83% | 100% |
C9ZV80 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 84% |
E9AWC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QB49 | Leishmania major | 81% | 100% |
V5BJC2 | Trypanosoma cruzi | 45% | 86% |