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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WUU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018095 | protein polyglutamylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016881 | acid-amino acid ligase activity | 4 | 1 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 1 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.247 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.243 |
DEG_APCC_DBOX_1 | 268 | 276 | PF00400 | 0.448 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.696 |
DOC_CYCLIN_RxL_1 | 330 | 337 | PF00134 | 0.473 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 302 | 311 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 124 | 132 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 237 | 245 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 237 | 245 | PF00069 | 0.434 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.448 |
DOC_PP4_MxPP_1 | 133 | 136 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.457 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 289 | 293 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 84 | 88 | PF12436 | 0.434 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 269 | 273 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.473 |
LIG_deltaCOP1_diTrp_1 | 155 | 160 | PF00928 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 36 | 43 | PF00928 | 0.327 |
LIG_EH1_1 | 335 | 343 | PF00400 | 0.490 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.434 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.325 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.466 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.545 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.309 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.360 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.434 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.438 |
LIG_LIR_Apic_2 | 109 | 113 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 211 | 216 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 260 | 270 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 392 | 399 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.375 |
LIG_OCRL_FandH_1 | 159 | 171 | PF00620 | 0.518 |
LIG_PCNA_PIPBox_1 | 329 | 338 | PF02747 | 0.518 |
LIG_PCNA_yPIPBox_3 | 329 | 340 | PF02747 | 0.518 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.434 |
LIG_Pex14_2 | 106 | 110 | PF04695 | 0.448 |
LIG_Pex14_2 | 119 | 123 | PF04695 | 0.448 |
LIG_Pex14_2 | 413 | 417 | PF04695 | 0.343 |
LIG_Rb_pABgroove_1 | 388 | 396 | PF01858 | 0.512 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.434 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 244 | 247 | PF00017 | 0.434 |
LIG_SH2_PTP2 | 279 | 282 | PF00017 | 0.524 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 222 | 225 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.428 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.484 |
LIG_SH3_4 | 134 | 141 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 20 | 26 | PF11976 | 0.308 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.544 |
LIG_UBA3_1 | 331 | 340 | PF00899 | 0.439 |
LIG_WW_3 | 453 | 457 | PF00397 | 0.432 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.448 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.553 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.520 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.394 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.434 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.522 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.234 |
MOD_Cter_Amidation | 400 | 403 | PF01082 | 0.528 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.297 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.339 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.319 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.241 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.545 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.453 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.434 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.590 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.518 |
MOD_LATS_1 | 3 | 9 | PF00433 | 0.613 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.234 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.576 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.604 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.434 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.524 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.322 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.443 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.421 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.490 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.434 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.517 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.473 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.434 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.664 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.531 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.564 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.259 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.446 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.546 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.434 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.434 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.518 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.459 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.441 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.524 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.319 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.473 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.490 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.434 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.526 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.459 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.518 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.434 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.434 |
MOD_SUMO_rev_2 | 155 | 162 | PF00179 | 0.514 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P402 | Leptomonas seymouri | 83% | 100% |
A0A1X0NFU6 | Trypanosomatidae | 35% | 88% |
A0A1X0NZP1 | Trypanosomatidae | 36% | 90% |
A0A1X0P705 | Trypanosomatidae | 65% | 100% |
A0A3R7MY56 | Trypanosoma rangeli | 65% | 100% |
A0A3S5IS28 | Trypanosoma rangeli | 25% | 73% |
A0A422N932 | Trypanosoma rangeli | 34% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 24% | 76% |
A2APC3 | Mus musculus | 46% | 100% |
A4H9E1 | Leishmania braziliensis | 90% | 98% |
A4HXR2 | Leishmania infantum | 95% | 99% |
B6DTF7 | Bodo saltans | 64% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 69% |
C9ZPR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 89% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 74% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 71% |
D0A044 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
O95922 | Homo sapiens | 39% | 100% |
P38160 | Sus scrofa | 25% | 100% |
P38584 | Bos taurus | 25% | 100% |
P38585 | Mus musculus | 24% | 100% |
Q0VC71 | Bos taurus | 39% | 100% |
Q23SI8 | Tetrahymena thermophila (strain SB210) | 38% | 100% |
Q3SXZ7 | Homo sapiens | 42% | 100% |
Q3SZH6 | Bos taurus | 45% | 100% |
Q4QE05 | Leishmania major | 93% | 99% |
Q564U4 | Caenorhabditis elegans | 41% | 100% |
Q5PPI9 | Rattus norvegicus | 39% | 100% |
Q641W7 | Rattus norvegicus | 45% | 100% |
Q8NG68 | Homo sapiens | 24% | 100% |
Q91V51 | Mus musculus | 39% | 100% |
Q9QXJ0 | Rattus norvegicus | 25% | 100% |
V5BVF5 | Trypanosoma cruzi | 23% | 73% |