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: 11 |
NetGPI | no | yes: 0, no: 11 |
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: A4I351
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
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 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
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_NRD_NRD_1 | 154 | 156 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 154 | 162 | PF00400 | 0.537 |
DEG_APCC_DBOX_1 | 319 | 327 | PF00400 | 0.491 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 421 | 425 | PF00917 | 0.548 |
DOC_CKS1_1 | 370 | 375 | PF01111 | 0.444 |
DOC_CYCLIN_RxL_1 | 309 | 321 | PF00134 | 0.543 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 239 | PF00134 | 0.451 |
DOC_MAPK_gen_1 | 180 | 187 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 223 | 229 | PF00069 | 0.453 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.376 |
DOC_SPAK_OSR1_1 | 82 | 86 | PF12202 | 0.371 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.406 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 65 | 72 | PF00244 | 0.452 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.354 |
LIG_BIR_III_2 | 466 | 470 | PF00653 | 0.484 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.626 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.494 |
LIG_Clathr_ClatBox_1 | 89 | 93 | PF01394 | 0.444 |
LIG_CSL_BTD_1 | 287 | 290 | PF09270 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 130 | 136 | PF00928 | 0.486 |
LIG_eIF4E_1 | 212 | 218 | PF01652 | 0.451 |
LIG_eIF4E_1 | 337 | 343 | PF01652 | 0.475 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.444 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.526 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.406 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.468 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.526 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.740 |
LIG_GBD_Chelix_1 | 318 | 326 | PF00786 | 0.343 |
LIG_Integrin_isoDGR_2 | 221 | 223 | PF01839 | 0.300 |
LIG_Integrin_RGD_1 | 464 | 466 | PF01839 | 0.491 |
LIG_LIR_Apic_2 | 368 | 373 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.377 |
LIG_PCNA_PIPBox_1 | 126 | 135 | PF02747 | 0.500 |
LIG_Pex14_1 | 106 | 110 | PF04695 | 0.338 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.381 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.472 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.451 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.376 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.537 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 207 | 210 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.520 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.451 |
LIG_SUMO_SIM_par_1 | 214 | 220 | PF11976 | 0.537 |
LIG_TYR_ITIM | 85 | 90 | PF00017 | 0.353 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.450 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.690 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.472 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.420 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.462 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.500 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.287 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.737 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.606 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.730 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.607 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.362 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.553 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.524 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.709 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.389 |
MOD_CMANNOS | 133 | 136 | PF00535 | 0.337 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.262 |
MOD_Cter_Amidation | 429 | 432 | PF01082 | 0.661 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.252 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.226 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.682 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.498 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.708 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.713 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.447 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.472 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.567 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.663 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.611 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.691 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.660 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.634 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.711 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.525 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.488 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.448 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.251 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.666 |
MOD_N-GLC_2 | 268 | 270 | PF02516 | 0.251 |
MOD_N-GLC_2 | 426 | 428 | PF02516 | 0.521 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.353 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.384 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.497 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.566 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.538 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.532 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.469 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.612 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.386 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.440 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.431 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.511 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.630 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.488 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.445 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.557 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.723 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.433 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.480 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.541 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.409 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.368 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.390 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.598 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.451 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.443 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.358 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.746 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.658 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.624 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_1 | 456 | 461 | PF01217 | 0.528 |
TRG_DiLeu_BaEn_2 | 453 | 459 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P402 | Leptomonas seymouri | 23% | 100% |
A0A0N1I1A1 | Leptomonas seymouri | 65% | 100% |
A0A0S4ISF0 | Bodo saltans | 25% | 84% |
A0A0S4J6I6 | Bodo saltans | 41% | 100% |
A0A1X0NFL2 | Trypanosomatidae | 51% | 100% |
A0A1X0NRN8 | Trypanosomatidae | 33% | 96% |
A0A1X0P6A0 | Trypanosomatidae | 25% | 71% |
A0A3Q8IDP1 | Leishmania donovani | 100% | 89% |
A0A422N932 | Trypanosoma rangeli | 24% | 100% |
A0A422NE52 | Trypanosoma rangeli | 49% | 100% |
A0A422P136 | Trypanosoma rangeli | 26% | 72% |
A4H9E1 | Leishmania braziliensis | 23% | 100% |
A4HG29 | Leishmania braziliensis | 79% | 100% |
A4Q9E4 | Mus musculus | 27% | 88% |
C9ZJM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9ACW9 | Leishmania major | 94% | 100% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
P38160 | Sus scrofa | 35% | 100% |
P38584 | Bos taurus | 34% | 100% |
P38585 | Mus musculus | 34% | 100% |
Q23SI8 | Tetrahymena thermophila (strain SB210) | 25% | 100% |
Q8NG68 | Homo sapiens | 35% | 100% |
Q9QXJ0 | Rattus norvegicus | 34% | 100% |
V5B4U2 | Trypanosoma cruzi | 23% | 86% |
V5D711 | Trypanosoma cruzi | 51% | 100% |