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: Q4Q709
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0043085 | positive regulation of catalytic activity | 4 | 2 |
GO:0043087 | regulation of GTPase activity | 5 | 2 |
GO:0043547 | positive regulation of GTPase activity | 6 | 2 |
GO:0044093 | positive regulation of molecular function | 3 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051336 | regulation of hydrolase activity | 4 | 2 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0090630 | activation of GTPase activity | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0003924 | GTPase activity | 7 | 5 |
GO:0003925 | G protein activity | 2 | 5 |
GO:0005096 | GTPase activator activity | 4 | 2 |
GO:0008047 | enzyme activator activity | 3 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 5 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 5 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 5 |
GO:0030234 | enzyme regulator activity | 2 | 2 |
GO:0030695 | GTPase regulator activity | 4 | 2 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 5 |
GO:0140677 | molecular function activator activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.359 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.491 |
DOC_CYCLIN_yClb1_LxF_4 | 171 | 177 | PF00134 | 0.447 |
DOC_MAPK_MEF2A_6 | 53 | 60 | PF00069 | 0.428 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.350 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.378 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.408 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.461 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.460 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 8 | 19 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.497 |
LIG_PDZ_Class_1 | 319 | 324 | PF00595 | 0.641 |
LIG_Pex14_1 | 277 | 281 | PF04695 | 0.400 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.445 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.355 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.355 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.441 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.466 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.463 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.383 |
LIG_TYR_ITIM | 185 | 190 | PF00017 | 0.402 |
LIG_UBA3_1 | 269 | 276 | PF00899 | 0.479 |
LIG_UBA3_1 | 285 | 290 | PF00899 | 0.396 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.335 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.424 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.482 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.558 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.430 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.391 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.557 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.434 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.529 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.364 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.408 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.480 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.461 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.355 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.391 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.566 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.432 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.298 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.378 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.417 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.558 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.398 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.480 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.388 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.313 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.480 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.403 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.572 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.466 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.350 |
MOD_SUMO_rev_2 | 282 | 292 | PF00179 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1N7 | Leptomonas seymouri | 66% | 100% |
A0A0S4ITU5 | Bodo saltans | 40% | 79% |
A0A1X0P1K5 | Trypanosomatidae | 47% | 81% |
A0A3S7X3S6 | Leishmania donovani | 95% | 100% |
A4HIL7 | Leishmania braziliensis | 81% | 100% |
A4I5W2 | Leishmania infantum | 95% | 100% |
C9ZR83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 82% |
E9B157 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5B7A5 | Trypanosoma cruzi | 50% | 100% |