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 | 2 |
GO:0005876 | spindle microtubule | 7 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0099081 | supramolecular polymer | 3 | 2 |
GO:0099512 | supramolecular fiber | 4 | 2 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACW9
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
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:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 3 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 3 |
GO:0016881 | acid-amino acid ligase activity | 4 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.536 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.539 |
DEG_APCC_DBOX_1 | 322 | 330 | PF00400 | 0.493 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.463 |
DOC_CKS1_1 | 373 | 378 | PF01111 | 0.447 |
DOC_CYCLIN_RxL_1 | 312 | 324 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.453 |
DOC_MAPK_gen_1 | 183 | 190 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 226 | 232 | PF00069 | 0.456 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.382 |
DOC_SPAK_OSR1_1 | 85 | 89 | PF12202 | 0.376 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.421 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.768 |
LIG_14-3-3_CanoR_1 | 100 | 104 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.360 |
LIG_APCC_ABBA_1 | 52 | 57 | PF00400 | 0.365 |
LIG_BIR_III_2 | 469 | 473 | PF00653 | 0.495 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 437 | 441 | PF00533 | 0.632 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 92 | 96 | PF01394 | 0.455 |
LIG_CSL_BTD_1 | 138 | 141 | PF09270 | 0.475 |
LIG_CSL_BTD_1 | 290 | 293 | PF09270 | 0.478 |
LIG_deltaCOP1_diTrp_1 | 133 | 139 | PF00928 | 0.489 |
LIG_eIF4E_1 | 215 | 221 | PF01652 | 0.453 |
LIG_eIF4E_1 | 340 | 346 | PF01652 | 0.478 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.458 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.528 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.409 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.473 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.529 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.765 |
LIG_GBD_Chelix_1 | 321 | 329 | PF00786 | 0.345 |
LIG_Integrin_isoDGR_2 | 224 | 226 | PF01839 | 0.303 |
LIG_Integrin_RGD_1 | 467 | 469 | PF01839 | 0.499 |
LIG_LIR_Apic_2 | 371 | 376 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 84 | 89 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 53 | 62 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.382 |
LIG_PCNA_PIPBox_1 | 129 | 138 | PF02747 | 0.503 |
LIG_PDZ_Class_3 | 474 | 479 | PF00595 | 0.357 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.340 |
LIG_Pex14_2 | 461 | 465 | PF04695 | 0.385 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.475 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.453 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.530 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.453 |
LIG_SUMO_SIM_anti_2 | 324 | 331 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.539 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.362 |
MOD_CDK_SPxxK_3 | 372 | 379 | PF00069 | 0.455 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.457 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.713 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.467 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.422 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.464 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.503 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.750 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.290 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.628 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.755 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.612 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.369 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.556 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.528 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.735 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.395 |
MOD_CMANNOS | 136 | 139 | PF00535 | 0.339 |
MOD_Cter_Amidation | 224 | 227 | PF01082 | 0.265 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.675 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.255 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.229 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.671 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.501 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.736 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.600 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.725 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.664 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.449 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.453 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.496 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.570 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.605 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.707 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.657 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.741 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.495 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.529 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.703 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.253 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.759 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.692 |
MOD_N-GLC_2 | 271 | 273 | PF02516 | 0.253 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.369 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.386 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.500 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.568 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.556 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.558 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.473 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.384 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.650 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.454 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.514 |
MOD_PKA_1 | 434 | 440 | PF00069 | 0.635 |
MOD_PKA_1 | 68 | 74 | PF00069 | 0.488 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.448 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.559 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.611 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.728 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.433 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.437 |
MOD_PKB_1 | 2 | 10 | PF00069 | 0.511 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.479 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.487 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.482 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.544 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.412 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.377 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.406 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.652 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.453 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.617 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.446 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.363 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.769 |
TRG_DiLeu_BaEn_1 | 156 | 161 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_2 | 456 | 462 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1A1 | Leptomonas seymouri | 67% | 100% |
A0A0S4ISF0 | Bodo saltans | 25% | 84% |
A0A0S4J6I6 | Bodo saltans | 39% | 100% |
A0A1X0NFL2 | Trypanosomatidae | 51% | 100% |
A0A1X0NRN8 | Trypanosomatidae | 31% | 97% |
A0A3Q8IDP1 | Leishmania donovani | 94% | 89% |
A0A422NE52 | Trypanosoma rangeli | 50% | 100% |
A0A422P136 | Trypanosoma rangeli | 26% | 73% |
A4H9E1 | Leishmania braziliensis | 22% | 100% |
A4HG29 | Leishmania braziliensis | 78% | 94% |
A4I351 | Leishmania infantum | 94% | 100% |
C9ZJM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P38160 | Sus scrofa | 35% | 100% |
P38584 | Bos taurus | 34% | 100% |
P38585 | Mus musculus | 35% | 100% |
Q10438 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q23SI8 | Tetrahymena thermophila (strain SB210) | 26% | 100% |
Q8NG68 | Homo sapiens | 35% | 100% |
Q9QXJ0 | Rattus norvegicus | 34% | 100% |
V5ARK1 | Trypanosoma cruzi | 24% | 100% |
V5B4U2 | Trypanosoma cruzi | 24% | 87% |
V5D711 | Trypanosoma cruzi | 51% | 100% |