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: A4HKT5
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:0004835 | tubulin-tyrosine ligase activity | 3 | 7 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 7 |
GO:0016881 | acid-amino acid ligase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 67 | 73 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 206 | 214 | PF00400 | 0.591 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.531 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.433 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.411 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.471 |
DOC_CKS1_1 | 375 | 380 | PF01111 | 0.549 |
DOC_CYCLIN_RxL_1 | 10 | 18 | PF00134 | 0.538 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.563 |
DOC_MAPK_gen_1 | 483 | 493 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 465 | 472 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.680 |
DOC_MAPK_NFAT4_5 | 465 | 473 | PF00069 | 0.561 |
DOC_PP1_RVXF_1 | 109 | 116 | PF00149 | 0.533 |
DOC_PP1_RVXF_1 | 209 | 216 | PF00149 | 0.561 |
DOC_PP1_SILK_1 | 207 | 212 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 98 | 101 | PF13499 | 0.697 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 120 | 125 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 266 | 271 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 91 | 96 | PF00244 | 0.680 |
LIG_Actin_WH2_2 | 109 | 127 | PF00022 | 0.449 |
LIG_APCC_ABBA_1 | 257 | 262 | PF00400 | 0.531 |
LIG_CaM_NSCaTE_8 | 445 | 452 | PF13499 | 0.531 |
LIG_eIF4E_1 | 230 | 236 | PF01652 | 0.490 |
LIG_eIF4E_1 | 258 | 264 | PF01652 | 0.508 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.362 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.451 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.537 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.522 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.587 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.560 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.495 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.529 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.443 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.494 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.614 |
LIG_LIR_Apic_2 | 90 | 96 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 426 | 437 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.447 |
LIG_LIR_LC3C_4 | 32 | 37 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.493 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.531 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.591 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.476 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.665 |
LIG_SH2_GRB2like | 135 | 138 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 93 | 97 | PF00017 | 0.629 |
LIG_SH2_PTP2 | 490 | 493 | PF00017 | 0.462 |
LIG_SH2_SRC | 304 | 307 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.217 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.628 |
LIG_SH3_2 | 453 | 458 | PF14604 | 0.561 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.411 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.561 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.551 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.518 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.558 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.561 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 92 | 99 | PF00069 | 0.730 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.487 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.665 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.547 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.762 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.597 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.506 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.488 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.571 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.311 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.310 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.654 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.470 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.418 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.568 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.480 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.508 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.687 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.616 |
MOD_N-GLC_2 | 291 | 293 | PF02516 | 0.290 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.484 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.516 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.508 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.535 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.507 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.646 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.344 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.571 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.531 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.632 |
MOD_PK_1 | 266 | 272 | PF00069 | 0.490 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.692 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.547 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.490 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.490 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.551 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.569 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.513 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.535 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.498 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.536 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.571 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.568 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.731 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.691 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 435 | 444 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_4 | 305 | 311 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.490 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M9 | Leptomonas seymouri | 70% | 77% |
A0A1X0NRN8 | Trypanosomatidae | 43% | 100% |
A0A3Q8IH06 | Leishmania donovani | 86% | 78% |
A0A422NE52 | Trypanosoma rangeli | 29% | 100% |
A0A422NZN7 | Trypanosoma rangeli | 41% | 96% |
A4I8B4 | Leishmania infantum | 86% | 100% |
E9B373 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q4Y1 | Leishmania major | 83% | 100% |