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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HPA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003727 | single-stranded RNA binding | 5 | 1 |
GO:0004521 | RNA endonuclease activity | 5 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.374 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.415 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.661 |
CLV_PCSK_PC7_1 | 9 | 15 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.588 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.469 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.520 |
DEG_SPOP_SBC_1 | 391 | 395 | PF00917 | 0.574 |
DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.320 |
DOC_MAPK_RevD_3 | 247 | 262 | PF00069 | 0.415 |
DOC_PP2B_LxvP_1 | 273 | 276 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 100 | 103 | PF00568 | 0.361 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.698 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.360 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 380 | 388 | PF00244 | 0.479 |
LIG_deltaCOP1_diTrp_1 | 141 | 149 | PF00928 | 0.368 |
LIG_deltaCOP1_diTrp_1 | 41 | 47 | PF00928 | 0.310 |
LIG_eIF4E_1 | 197 | 203 | PF01652 | 0.415 |
LIG_eIF4E_1 | 382 | 388 | PF01652 | 0.479 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.488 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.228 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.415 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.450 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.464 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.471 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 265 | 273 | PF00786 | 0.271 |
LIG_GBD_Chelix_1 | 355 | 363 | PF00786 | 0.271 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.471 |
LIG_LYPXL_yS_3 | 197 | 200 | PF13949 | 0.471 |
LIG_PCNA_PIPBox_1 | 200 | 209 | PF02747 | 0.415 |
LIG_SH2_PTP2 | 344 | 347 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.538 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.366 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.471 |
LIG_Sin3_3 | 356 | 363 | PF02671 | 0.471 |
LIG_SUMO_SIM_par_1 | 248 | 253 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.415 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.430 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.346 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.455 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.359 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.395 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.223 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.482 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.541 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.431 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.470 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.399 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.471 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.471 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.526 |
MOD_CMANNOS | 44 | 47 | PF00535 | 0.497 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.271 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.641 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.385 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.416 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.697 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.470 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.451 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.228 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.459 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.472 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.465 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.503 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.407 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.415 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.529 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.437 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.609 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.361 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.228 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.497 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.480 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.596 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.471 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.455 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.520 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.520 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.471 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.398 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.471 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.530 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.473 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.426 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.456 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.471 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.359 |
MOD_SUMO_rev_2 | 72 | 78 | PF00179 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.325 |
TRG_NES_CRM1_1 | 50 | 64 | PF08389 | 0.271 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN9 | Leptomonas seymouri | 52% | 100% |
A0A3S7XAV3 | Leishmania donovani | 71% | 100% |
A4IDK7 | Leishmania infantum | 71% | 100% |
E9AT10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 99% |
Q4Q1I8 | Leishmania major | 71% | 100% |