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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006284 | base-excision repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004519 | endonuclease activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008309 | double-stranded DNA exodeoxyribonuclease activity | 7 | 1 |
GO:0008311 | double-stranded DNA 3'-5' DNA exonuclease activity | 8 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.184 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.613 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.758 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.229 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 298 | 306 | PF00400 | 0.261 |
DEG_COP1_1 | 310 | 318 | PF00400 | 0.294 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 402 | 410 | PF00134 | 0.346 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.547 |
DOC_PP1_RVXF_1 | 129 | 136 | PF00149 | 0.292 |
DOC_PP1_RVXF_1 | 402 | 409 | PF00149 | 0.280 |
DOC_PP4_FxxP_1 | 224 | 227 | PF00568 | 0.391 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.373 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.261 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.432 |
DOC_USP7_MATH_2 | 362 | 368 | PF00917 | 0.261 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 117 | 124 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 365 | 369 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 418 | 423 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.650 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_deltaCOP1_diTrp_1 | 107 | 115 | PF00928 | 0.495 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.290 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.340 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.289 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.275 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.603 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.474 |
LIG_Integrin_isoDGR_2 | 400 | 402 | PF01839 | 0.280 |
LIG_LIR_Apic_2 | 221 | 227 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 254 | 259 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 425 | 430 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.261 |
LIG_MAD2 | 251 | 259 | PF02301 | 0.373 |
LIG_NRBOX | 139 | 145 | PF00104 | 0.280 |
LIG_PCNA_yPIPBox_3 | 80 | 90 | PF02747 | 0.399 |
LIG_Pex14_1 | 408 | 412 | PF04695 | 0.273 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.261 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.261 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.349 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.346 |
LIG_SUMO_SIM_anti_2 | 265 | 275 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.281 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.294 |
LIG_TRAF2_1 | 361 | 364 | PF00917 | 0.228 |
LIG_TYR_ITIM | 410 | 415 | PF00017 | 0.261 |
LIG_UBA3_1 | 162 | 169 | PF00899 | 0.180 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 391 | 396 | PF05994 | 0.324 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.774 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.754 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.415 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.391 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.479 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.294 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.207 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.297 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.277 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.408 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.299 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.390 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.285 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.717 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.625 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.645 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.621 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.287 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.320 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.417 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.294 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.247 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.310 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.634 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.228 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.681 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.781 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.346 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.420 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.271 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.391 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.280 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.280 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.244 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.261 |
MOD_NEK2_2 | 347 | 352 | PF00069 | 0.391 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.408 |
MOD_PK_1 | 374 | 380 | PF00069 | 0.346 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.675 |
MOD_PKA_1 | 63 | 69 | PF00069 | 0.753 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.652 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.387 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.432 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.270 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.613 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.695 |
MOD_PKB_1 | 5 | 13 | PF00069 | 0.677 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.346 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.420 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.346 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.355 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.362 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.265 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.284 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.280 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.401 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.378 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.636 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.308 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.387 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.305 |
MOD_SUMO_for_1 | 38 | 41 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 161 | 170 | PF00179 | 0.261 |
TRG_DiLeu_BaEn_4 | 248 | 254 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.261 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.561 |
TRG_NLS_MonoCore_2 | 3 | 8 | PF00514 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 382 | 387 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIW7 | Leptomonas seymouri | 65% | 100% |
A0A0S4JDZ9 | Bodo saltans | 48% | 100% |
A0A3R7KY33 | Trypanosoma rangeli | 57% | 99% |
A0A3S7WTW9 | Leishmania donovani | 91% | 100% |
A0MTA1 | Danio rerio | 33% | 100% |
A1YES6 | Gorilla gorilla gorilla | 33% | 100% |
A1YFZ3 | Pan paniscus | 33% | 100% |
A2T6Y4 | Pan troglodytes | 33% | 100% |
A2T7I6 | Pongo pygmaeus | 33% | 100% |
A4H8J0 | Leishmania braziliensis | 85% | 99% |
C9ZW21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AGN4 | Leishmania infantum | 92% | 100% |
O15922 | Leishmania major | 92% | 100% |
P23196 | Bos taurus | 32% | 100% |
P27695 | Homo sapiens | 34% | 100% |
P28352 | Mus musculus | 32% | 100% |
P43138 | Rattus norvegicus | 32% | 100% |
P45951 | Arabidopsis thaliana | 31% | 83% |
P51173 | Dictyostelium discoideum | 34% | 100% |
P87175 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 85% |
Q5XF07 | Arabidopsis thaliana | 24% | 100% |
Q9UBZ4 | Homo sapiens | 28% | 86% |
V5AT33 | Trypanosoma cruzi | 58% | 100% |