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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4I5W2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043087 | regulation of GTPase activity | 5 | 1 |
GO:0043547 | positive regulation of GTPase activity | 6 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051336 | regulation of hydrolase activity | 4 | 1 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0090630 | activation of GTPase activity | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0003924 | GTPase activity | 7 | 5 |
GO:0003925 | G protein activity | 2 | 5 |
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:0098772 | molecular function regulator activity | 1 | 5 |
GO:0005096 | GTPase activator activity | 4 | 1 |
GO:0008047 | enzyme activator activity | 3 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030695 | GTPase regulator activity | 4 | 1 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 1 |
GO:0140677 | molecular function activator activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.256 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.275 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.424 |
DOC_CYCLIN_yClb1_LxF_4 | 171 | 177 | PF00134 | 0.386 |
DOC_MAPK_MEF2A_6 | 53 | 60 | PF00069 | 0.386 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.275 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.240 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.294 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.279 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.300 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.335 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.406 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.462 |
LIG_LIR_Gen_1 | 180 | 190 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 8 | 19 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.474 |
LIG_PDZ_Class_1 | 319 | 324 | PF00595 | 0.546 |
LIG_Pex14_1 | 217 | 221 | PF04695 | 0.188 |
LIG_Pex14_1 | 277 | 281 | PF04695 | 0.319 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.383 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.259 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.120 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.284 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.431 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.385 |
LIG_TYR_ITIM | 185 | 190 | PF00017 | 0.262 |
LIG_UBA3_1 | 269 | 276 | PF00899 | 0.416 |
LIG_UBA3_1 | 285 | 290 | PF00899 | 0.410 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.256 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.355 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.426 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.341 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.503 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.363 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.315 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.434 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.368 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.416 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.304 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.335 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.412 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.406 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.275 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.324 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.536 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.367 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.214 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.300 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.350 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.390 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.396 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.335 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.412 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.326 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.264 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.454 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.357 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.464 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.390 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.294 |
MOD_SUMO_rev_2 | 282 | 292 | PF00179 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.256 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1N7 | Leptomonas seymouri | 67% | 100% |
A0A0S4ITU5 | Bodo saltans | 40% | 79% |
A0A1X0NLM2 | Trypanosomatidae | 25% | 92% |
A0A1X0P1K5 | Trypanosomatidae | 47% | 81% |
A0A1X0P278 | Trypanosomatidae | 27% | 79% |
A0A1X0P2Z0 | Trypanosomatidae | 20% | 72% |
A0A3S7X3S6 | Leishmania donovani | 99% | 100% |
A0A422NJ84 | Trypanosoma rangeli | 27% | 77% |
A4HIL7 | Leishmania braziliensis | 82% | 100% |
A4HQC7 | Leishmania braziliensis | 25% | 76% |
C9ZR83 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 82% |
E9ARB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 67% |
E9B157 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
P36618 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q4Q0F2 | Leishmania major | 24% | 78% |
Q4Q709 | Leishmania major | 95% | 100% |
Q6PBU5 | Danio rerio | 25% | 91% |
V5B7A5 | Trypanosoma cruzi | 51% | 100% |
V5BT66 | Trypanosoma cruzi | 27% | 79% |
V5BU55 | Trypanosoma cruzi | 24% | 71% |
V5DK04 | Trypanosoma cruzi | 27% | 100% |