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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 1 |
GO:0005876 | spindle microtubule | 7 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HG29
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
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:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 2 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 2 |
GO:0016881 | acid-amino acid ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 124 | 130 | PF00089 | 0.288 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.515 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.211 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.419 |
CLV_PCSK_PC7_1 | 177 | 183 | PF00082 | 0.176 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.454 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.526 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.307 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.487 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.495 |
DOC_CYCLIN_yClb3_PxF_3 | 4 | 10 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 260 | 266 | PF00134 | 0.455 |
DOC_MAPK_gen_1 | 250 | 256 | PF00069 | 0.458 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.383 |
DOC_SPAK_OSR1_1 | 109 | 113 | PF12202 | 0.377 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 142 | 146 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 215 | 223 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 464 | 472 | PF00244 | 0.698 |
LIG_APCC_ABBA_1 | 76 | 81 | PF00400 | 0.361 |
LIG_BIR_III_2 | 410 | 414 | PF00653 | 0.413 |
LIG_BIR_III_2 | 494 | 498 | PF00653 | 0.501 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.500 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.494 |
LIG_CSL_BTD_1 | 162 | 165 | PF09270 | 0.473 |
LIG_CSL_BTD_1 | 314 | 317 | PF09270 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 157 | 163 | PF00928 | 0.502 |
LIG_eIF4E_1 | 239 | 245 | PF01652 | 0.455 |
LIG_eIF4E_1 | 364 | 370 | PF01652 | 0.473 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.450 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.449 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.434 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.330 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.511 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.703 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.545 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.417 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.730 |
LIG_GBD_Chelix_1 | 345 | 353 | PF00786 | 0.344 |
LIG_IRF3_LxIS_1 | 223 | 229 | PF10401 | 0.376 |
LIG_LIR_Apic_2 | 108 | 113 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 483 | 492 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.365 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.496 |
LIG_Pex14_2 | 486 | 490 | PF04695 | 0.390 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.428 |
LIG_Rb_pABgroove_1 | 403 | 411 | PF01858 | 0.293 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.395 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 269 | 273 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.526 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.512 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 234 | 237 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.439 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.413 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.455 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 348 | 354 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 241 | 247 | PF11976 | 0.526 |
LIG_TYR_ITIM | 112 | 117 | PF00017 | 0.361 |
LIG_WRC_WIRS_1 | 10 | 15 | PF05994 | 0.432 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.371 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.499 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.472 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.429 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.689 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.567 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.675 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.385 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.434 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.725 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.615 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.543 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.403 |
MOD_CMANNOS | 160 | 163 | PF00535 | 0.326 |
MOD_Cter_Amidation | 248 | 251 | PF01082 | 0.274 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.378 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.255 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.255 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.203 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.466 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.746 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.713 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.397 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.456 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.473 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.391 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.720 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.730 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.538 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.428 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.444 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.255 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.658 |
MOD_N-GLC_2 | 295 | 297 | PF02516 | 0.255 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.480 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.374 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.427 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.382 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.476 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.565 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.528 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.496 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.416 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.739 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.382 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.372 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.556 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.416 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.476 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.390 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.438 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.556 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.721 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.430 |
MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.376 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.521 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.466 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.428 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.428 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.398 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.473 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.455 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.428 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.773 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.768 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 378 | 385 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_1 | 484 | 489 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_2 | 481 | 487 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 240 | 245 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1A1 | Leptomonas seymouri | 63% | 100% |
A0A0S4J6I6 | Bodo saltans | 41% | 100% |
A0A1X0NRN8 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDP1 | Leishmania donovani | 79% | 95% |
A0A422NE52 | Trypanosoma rangeli | 51% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 27% | 83% |
A4H9E1 | Leishmania braziliensis | 22% | 100% |
A4HXR2 | Leishmania infantum | 21% | 100% |
A4I351 | Leishmania infantum | 79% | 100% |
C9ZJM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9ACW9 | Leishmania major | 78% | 100% |
E9AID0 | Leishmania braziliensis | 24% | 68% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 20% | 100% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 71% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
P38160 | Sus scrofa | 37% | 100% |
P38584 | Bos taurus | 37% | 100% |
P38585 | Mus musculus | 35% | 100% |
Q4QE05 | Leishmania major | 21% | 100% |
Q8NG68 | Homo sapiens | 37% | 100% |
Q9QXJ0 | Rattus norvegicus | 35% | 100% |
V5BVF5 | Trypanosoma cruzi | 28% | 79% |