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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005776 | autophagosome | 6 | 1 |
GO:0010008 | endosome membrane | 5 | 1 |
GO:0012506 | vesicle membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0035869 | ciliary transition zone | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQE5
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007033 | vacuole organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1905037 | autophagosome organization | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0003924 | GTPase activity | 7 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005525 | GTP binding | 5 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0019001 | guanyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.296 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.254 |
DOC_MAPK_gen_1 | 273 | 280 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.290 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.274 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.193 |
DOC_USP7_MATH_2 | 2 | 8 | PF00917 | 0.345 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.547 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.597 |
DOC_USP7_UBL2_3 | 291 | 295 | PF12436 | 0.617 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 149 | 156 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 52 | 62 | PF00244 | 0.334 |
LIG_EVH1_1 | 233 | 237 | PF00568 | 0.487 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.366 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.277 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.553 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.507 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.250 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.274 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.274 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.294 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.450 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.205 |
LIG_LIR_Gen_1 | 69 | 79 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 95 | 102 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.254 |
LIG_NRBOX | 293 | 299 | PF00104 | 0.455 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.284 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.303 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 276 | 282 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 276 | 282 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 9 | 15 | PF11976 | 0.334 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.496 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.429 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.474 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.274 |
MOD_CAAXbox | 296 | 299 | PF01239 | 0.527 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.483 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.276 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.254 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.274 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.430 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.259 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.494 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.643 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.500 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.639 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.631 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.679 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.303 |
MOD_LATS_1 | 288 | 294 | PF00433 | 0.475 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.247 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.530 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.642 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.303 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.274 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.274 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.274 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.307 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.230 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.274 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.193 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.303 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.439 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.274 |
MOD_PK_1 | 106 | 112 | PF00069 | 0.334 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.471 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.314 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.770 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.354 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.334 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.373 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.247 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.302 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.247 |
MOD_Plk_2-3 | 176 | 182 | PF00069 | 0.452 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.317 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.508 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.274 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.669 |
MOD_SUMO_rev_2 | 261 | 271 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_2 | 45 | 51 | PF01217 | 0.334 |
TRG_NLS_MonoExtN_4 | 237 | 244 | PF00514 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IC49 | Leptomonas seymouri | 57% | 96% |
A0A0N1IKL4 | Leptomonas seymouri | 28% | 72% |
A0A0S4J9T5 | Bodo saltans | 25% | 100% |
A0A1X0NQ87 | Trypanosomatidae | 29% | 81% |
A0A1X0NUW7 | Trypanosomatidae | 26% | 100% |
A0A1X0P706 | Trypanosomatidae | 29% | 100% |
A0A3Q8I8T8 | Leishmania donovani | 34% | 100% |
A0A3Q8ICX9 | Leishmania donovani | 32% | 100% |
A0A3Q8ID64 | Leishmania donovani | 32% | 100% |
A0A3Q8IE68 | Leishmania donovani | 35% | 100% |
A0A3Q8IK84 | Leishmania donovani | 35% | 100% |
A0A3Q8IRV7 | Leishmania donovani | 67% | 100% |
A0A3R7KA22 | Trypanosoma rangeli | 67% | 100% |
A0A3R7LYA6 | Trypanosoma rangeli | 26% | 100% |
A0A3S5H4Z2 | Leishmania donovani | 33% | 100% |
A0A3S5H5Y5 | Leishmania donovani | 33% | 100% |
A0A3S5H6H3 | Leishmania donovani | 30% | 100% |
A0A3S7WRA9 | Leishmania donovani | 31% | 100% |
A0A3S7WUY8 | Leishmania donovani | 34% | 100% |
A0A3S7WV84 | Leishmania donovani | 28% | 100% |
A0A3S7X3D1 | Leishmania donovani | 28% | 100% |
A0A3S7X5J2 | Leishmania donovani | 33% | 100% |
A0A422NH56 | Trypanosoma rangeli | 27% | 100% |
A1KXP5 | Leishmania donovani | 29% | 100% |
A4H506 | Leishmania braziliensis | 31% | 100% |
A4H679 | Leishmania braziliensis | 31% | 100% |
A4H6A4 | Leishmania braziliensis | 34% | 100% |
A4H6A5 | Leishmania braziliensis | 30% | 100% |
A4H9M3 | Leishmania braziliensis | 28% | 100% |
A4HEE8 | Leishmania braziliensis | 29% | 100% |
A4HFK0 | Leishmania braziliensis | 34% | 100% |
A4HHR8 | Leishmania braziliensis | 29% | 100% |
A4HIB4 | Leishmania braziliensis | 33% | 100% |
A4HK33 | Leishmania braziliensis | 35% | 100% |
A4HKH2 | Leishmania braziliensis | 33% | 100% |
A4HKJ3 | Leishmania braziliensis | 32% | 100% |
A4HLP5 | Leishmania braziliensis | 35% | 100% |
A4HRM3 | Leishmania infantum | 33% | 100% |
A4HT72 | Leishmania infantum | 33% | 100% |
A4HUK3 | Leishmania infantum | 31% | 100% |
A4HUM8 | Leishmania infantum | 34% | 100% |
A4HUM9 | Leishmania infantum | 30% | 100% |
A4HVF7 | Leishmania infantum | 28% | 100% |
A4HXY7 | Leishmania infantum | 28% | 100% |
A4I1I6 | Leishmania infantum | 29% | 100% |
A4I5J8 | Leishmania infantum | 28% | 100% |
A4I7N3 | Leishmania infantum | 32% | 100% |
A4I7Z9 | Leishmania infantum | 33% | 100% |
A4I825 | Leishmania infantum | 32% | 100% |
A4I946 | Leishmania infantum | 35% | 100% |
A4IC86 | Leishmania infantum | 67% | 100% |
B1A5Z4 | Leishmania donovani | 29% | 100% |
C9ZVR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0AA91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AD53 | Leishmania major | 35% | 100% |
E9AGQ4 | Leishmania infantum | 34% | 100% |
E9AHE8 | Leishmania infantum | 35% | 100% |
E9AJI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AL68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9ANA1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ANC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ANC7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AP56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9ARM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ARQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AU60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9AXM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AYX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B0U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B2H2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B2W1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B2Y3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B420 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O04486 | Arabidopsis thaliana | 34% | 100% |
P01119 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 97% |
P09527 | Rattus norvegicus | 32% | 100% |
P20338 | Homo sapiens | 28% | 100% |
P35288 | Mus musculus | 38% | 100% |
P36018 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P61017 | Canis lupus familiaris | 30% | 100% |
P61018 | Homo sapiens | 30% | 100% |
P61028 | Mus musculus | 29% | 100% |
P70550 | Rattus norvegicus | 29% | 100% |
P97950 | Mus musculus | 32% | 100% |
Q06AU4 | Sus scrofa | 35% | 100% |
Q06AU5 | Sus scrofa | 31% | 100% |
Q0WQN4 | Arabidopsis thaliana | 31% | 100% |
Q14088 | Homo sapiens | 32% | 100% |
Q20365 | Caenorhabditis elegans | 28% | 97% |
Q2HJI8 | Bos taurus | 29% | 100% |
Q2TBH7 | Bos taurus | 28% | 100% |
Q4Q0D5 | Leishmania major | 66% | 100% |
Q4Q404 | Leishmania major | 34% | 100% |
Q4Q573 | Leishmania major | 32% | 100% |
Q4Q595 | Leishmania major | 33% | 100% |
Q4Q5N4 | Leishmania major | 36% | 100% |
Q4Q7C3 | Leishmania major | 32% | 100% |
Q4Q9V1 | Leishmania major | 29% | 100% |
Q4QDS9 | Leishmania major | 28% | 100% |
Q4QGD2 | Leishmania major | 29% | 100% |
Q4QH97 | Leishmania major | 30% | 100% |
Q4QH98 | Leishmania major | 34% | 100% |
Q4QHC3 | Leishmania major | 32% | 100% |
Q4QIN6 | Leishmania major | 33% | 100% |
Q53S08 | Homo sapiens | 31% | 100% |
Q54QR3 | Dictyostelium discoideum | 32% | 100% |
Q5REC9 | Pongo abelii | 29% | 100% |
Q5U1Y1 | Rattus norvegicus | 32% | 100% |
Q64008 | Mus musculus | 32% | 100% |
Q6PHI9 | Danio rerio | 28% | 100% |
Q8SS11 | Encephalitozoon cuniculi (strain GB-M1) | 29% | 100% |
Q92930 | Homo sapiens | 29% | 100% |
Q99260 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q99P58 | Mus musculus | 30% | 100% |
Q9BZG1 | Homo sapiens | 34% | 100% |
Q9H0N0 | Homo sapiens | 30% | 100% |
Q9N2P5 | Leishmania major | 34% | 100% |
Q9ULC3 | Homo sapiens | 39% | 100% |