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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AM46
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 9 |
GO:0008047 | enzyme activator activity | 3 | 9 |
GO:0030234 | enzyme regulator activity | 2 | 9 |
GO:0030695 | GTPase regulator activity | 4 | 9 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 9 |
GO:0098772 | molecular function regulator activity | 1 | 9 |
GO:0140677 | molecular function activator activity | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.702 |
CLV_PCSK_FUR_1 | 316 | 320 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.541 |
CLV_PCSK_PC7_1 | 279 | 285 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.438 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.377 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 204 | 213 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 164 | 173 | PF00069 | 0.184 |
DOC_MAPK_gen_1 | 316 | 323 | PF00069 | 0.350 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.511 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.760 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.628 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.663 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 113 | 118 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.370 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.671 |
LIG_deltaCOP1_diTrp_1 | 314 | 324 | PF00928 | 0.515 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.655 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.484 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.317 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.319 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.549 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.572 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.791 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.583 |
LIG_Integrin_RGD_1 | 262 | 264 | PF01839 | 0.590 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.572 |
LIG_PDZ_Class_2 | 384 | 389 | PF00595 | 0.683 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.516 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.184 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.680 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.550 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.558 |
LIG_SUMO_SIM_par_1 | 319 | 326 | PF11976 | 0.525 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.524 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.466 |
LIG_UBA3_1 | 156 | 164 | PF00899 | 0.294 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.263 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.629 |
MOD_CDC14_SPxK_1 | 241 | 244 | PF00782 | 0.553 |
MOD_CDK_SPxK_1 | 238 | 244 | PF00069 | 0.553 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.607 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.587 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.478 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.317 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.268 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.590 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.535 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.768 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.786 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.715 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.643 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.630 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.312 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.428 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.550 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.590 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.706 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.638 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.772 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.487 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.283 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.283 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.674 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.735 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.478 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.572 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.694 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.524 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.304 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.283 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.631 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.316 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.281 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.377 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.377 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.763 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.707 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.604 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.738 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.539 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.478 |
MOD_Plk_2-3 | 147 | 153 | PF00069 | 0.377 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.508 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.354 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.588 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.680 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.638 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.627 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.531 |
TRG_NLS_MonoCore_2 | 48 | 53 | PF00514 | 0.504 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.548 |
TRG_NLS_MonoExtN_4 | 48 | 55 | PF00514 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7F7 | Leptomonas seymouri | 61% | 100% |
A0A1X0NZE9 | Trypanosomatidae | 45% | 100% |
A0A3Q8IE49 | Leishmania donovani | 88% | 100% |
A4HH34 | Leishmania braziliensis | 68% | 100% |
A4I485 | Leishmania infantum | 88% | 100% |
C9ZKP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ADN4 | Leishmania major | 85% | 99% |