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 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4QE05
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0018095 | protein polyglutamylation | 7 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 2 |
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:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 2 |
GO:0016881 | acid-amino acid ligase activity | 4 | 2 |
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:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.229 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.216 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.229 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.443 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.689 |
DOC_CYCLIN_RxL_1 | 326 | 333 | PF00134 | 0.461 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 298 | 307 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 124 | 132 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.445 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 447 | 450 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.443 |
DOC_PP4_MxPP_1 | 133 | 136 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.429 |
DOC_USP7_UBL2_3 | 84 | 88 | PF12436 | 0.429 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 265 | 269 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.461 |
LIG_deltaCOP1_diTrp_1 | 155 | 160 | PF00928 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 36 | 43 | PF00928 | 0.320 |
LIG_EH1_1 | 331 | 339 | PF00400 | 0.485 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.433 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.528 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.468 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.531 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.302 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.353 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.429 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 109 | 113 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 207 | 212 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 272 | 283 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 388 | 395 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.367 |
LIG_OCRL_FandH_1 | 159 | 171 | PF00620 | 0.502 |
LIG_PCNA_PIPBox_1 | 325 | 334 | PF02747 | 0.502 |
LIG_PCNA_yPIPBox_3 | 325 | 336 | PF02747 | 0.502 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.429 |
LIG_Pex14_2 | 106 | 110 | PF04695 | 0.443 |
LIG_Pex14_2 | 119 | 123 | PF04695 | 0.443 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.338 |
LIG_Rb_pABgroove_1 | 384 | 392 | PF01858 | 0.508 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.429 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 240 | 243 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 275 | 278 | PF00017 | 0.520 |
LIG_SH2_SRC | 275 | 278 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.437 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.479 |
LIG_SH3_4 | 134 | 141 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 20 | 26 | PF11976 | 0.301 |
LIG_TRAF2_1 | 400 | 403 | PF00917 | 0.540 |
LIG_UBA3_1 | 327 | 336 | PF00899 | 0.434 |
LIG_WW_3 | 449 | 453 | PF00397 | 0.426 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.443 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.550 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.386 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.426 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.520 |
MOD_Cter_Amidation | 231 | 234 | PF01082 | 0.229 |
MOD_Cter_Amidation | 396 | 399 | PF01082 | 0.523 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.293 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.372 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.312 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.232 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.219 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.544 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.447 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.429 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.572 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.411 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.502 |
MOD_LATS_1 | 3 | 9 | PF00433 | 0.607 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.229 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.429 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.502 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.315 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.439 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.402 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.485 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.438 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.530 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.461 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.429 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.526 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.502 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.254 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.429 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.538 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.426 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.429 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.502 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.454 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.435 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.520 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.325 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.461 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.485 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.429 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.388 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.456 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.502 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.429 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.429 |
MOD_SUMO_rev_2 | 155 | 162 | PF00179 | 0.510 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P402 | Leptomonas seymouri | 84% | 100% |
A0A0N1I1A1 | Leptomonas seymouri | 23% | 100% |
A0A0N1IH77 | Leptomonas seymouri | 23% | 83% |
A0A0S4JEF0 | Bodo saltans | 39% | 100% |
A0A0S4KQK8 | Bodo saltans | 25% | 71% |
A0A1X0NFL2 | Trypanosomatidae | 21% | 100% |
A0A1X0NFU6 | Trypanosomatidae | 36% | 88% |
A0A1X0NZP1 | Trypanosomatidae | 36% | 89% |
A0A1X0P6A0 | Trypanosomatidae | 24% | 70% |
A0A1X0P705 | Trypanosomatidae | 65% | 100% |
A0A3R7MY56 | Trypanosoma rangeli | 66% | 100% |
A0A3S5IS28 | Trypanosoma rangeli | 25% | 72% |
A0A3S7WUU3 | Leishmania donovani | 93% | 99% |
A0A422N932 | Trypanosoma rangeli | 34% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 25% | 75% |
A0A422P136 | Trypanosoma rangeli | 24% | 71% |
A2APC3 | Mus musculus | 47% | 100% |
A4H9E1 | Leishmania braziliensis | 90% | 100% |
A4HG29 | Leishmania braziliensis | 21% | 91% |
A4HH59 | Leishmania braziliensis | 22% | 100% |
A4HXR2 | Leishmania infantum | 98% | 100% |
A4Q9E4 | Mus musculus | 25% | 86% |
B6DTF7 | Bodo saltans | 64% | 100% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 68% |
C9ZJM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
C9ZPR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 89% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 73% |
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) | 94% | 100% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 97% |
O95922 | Homo sapiens | 40% | 100% |
P38160 | Sus scrofa | 25% | 100% |
P38584 | Bos taurus | 25% | 100% |
P38585 | Mus musculus | 24% | 100% |
Q0VC71 | Bos taurus | 40% | 100% |
Q23SI8 | Tetrahymena thermophila (strain SB210) | 39% | 100% |
Q3SXZ7 | Homo sapiens | 43% | 100% |
Q3SZH6 | Bos taurus | 46% | 100% |
Q564U4 | Caenorhabditis elegans | 42% | 100% |
Q5PPI9 | Rattus norvegicus | 40% | 100% |
Q641W7 | Rattus norvegicus | 46% | 100% |
Q6ZVT0 | Homo sapiens | 24% | 69% |
Q8NG68 | Homo sapiens | 24% | 100% |
Q91V51 | Mus musculus | 40% | 100% |
Q9QXJ0 | Rattus norvegicus | 25% | 100% |
V5ARK1 | Trypanosoma cruzi | 24% | 99% |
V5BVF5 | Trypanosoma cruzi | 23% | 72% |
V5D711 | Trypanosoma cruzi | 23% | 100% |