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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: A0A3Q8IDP1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
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 | 9 |
GO:0016874 | ligase activity | 2 | 9 |
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 | 125 | 127 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.789 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.649 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.533 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.509 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.582 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.580 |
DOC_CDC14_PxL_1 | 16 | 24 | PF14671 | 0.407 |
DOC_CKS1_1 | 430 | 435 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 369 | 381 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 240 | 247 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 283 | 289 | PF00069 | 0.476 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.412 |
DOC_PP4_FxxP_1 | 143 | 146 | PF00568 | 0.405 |
DOC_PP4_FxxP_1 | 430 | 433 | PF00568 | 0.475 |
DOC_SPAK_OSR1_1 | 142 | 146 | PF12202 | 0.400 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 125 | 132 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 491 | 498 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 62 | 71 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 43 | 59 | PF00022 | 0.415 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.383 |
LIG_BIR_III_2 | 526 | 530 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.660 |
LIG_Clathr_ClatBox_1 | 149 | 153 | PF01394 | 0.463 |
LIG_CSL_BTD_1 | 347 | 350 | PF09270 | 0.499 |
LIG_deltaCOP1_diTrp_1 | 190 | 196 | PF00928 | 0.506 |
LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.475 |
LIG_eIF4E_1 | 397 | 403 | PF01652 | 0.499 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.456 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.411 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.518 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.561 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.481 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.558 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.745 |
LIG_GBD_Chelix_1 | 378 | 386 | PF00786 | 0.371 |
LIG_Integrin_isoDGR_2 | 281 | 283 | PF01839 | 0.316 |
LIG_Integrin_RGD_1 | 524 | 526 | PF01839 | 0.510 |
LIG_LIR_Apic_2 | 141 | 146 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 110 | 119 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.554 |
LIG_MYND_1 | 7 | 11 | PF01753 | 0.392 |
LIG_PCNA_PIPBox_1 | 186 | 195 | PF02747 | 0.516 |
LIG_Pex14_1 | 166 | 170 | PF04695 | 0.412 |
LIG_Pex14_2 | 518 | 522 | PF04695 | 0.433 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.391 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.488 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 302 | 306 | PF00017 | 0.533 |
LIG_SH2_SRC | 201 | 204 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 297 | 301 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.499 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.475 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.448 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.533 |
LIG_TYR_ITIM | 145 | 150 | PF00017 | 0.383 |
MOD_CDK_SPxxK_3 | 429 | 436 | PF00069 | 0.466 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.392 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.497 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.442 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.482 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.516 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.739 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.546 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.748 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.593 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.750 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.416 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.406 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.488 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.531 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.743 |
MOD_CMANNOS | 193 | 196 | PF00535 | 0.333 |
MOD_Cter_Amidation | 281 | 284 | PF01082 | 0.300 |
MOD_Cter_Amidation | 489 | 492 | PF01082 | 0.688 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.276 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.236 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.743 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.722 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.680 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.505 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.430 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.524 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.463 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.448 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.516 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.450 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.731 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.683 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.566 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.737 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.520 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.645 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.583 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.657 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.275 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.711 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.275 |
MOD_N-GLC_2 | 486 | 488 | PF02516 | 0.556 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.415 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.461 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.378 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.403 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.506 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.579 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.474 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.535 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.526 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.470 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.512 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.666 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.446 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.571 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.505 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.659 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.434 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.470 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.571 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.752 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.398 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.357 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.489 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.516 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.435 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.415 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.499 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.475 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.405 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.760 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.648 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.697 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.448 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.597 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_1 | 516 | 521 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_2 | 513 | 519 | PF01217 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 273 | 278 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 413 | 418 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1A1 | Leptomonas seymouri | 65% | 100% |
A0A0S4ISF0 | Bodo saltans | 25% | 94% |
A0A0S4J6I6 | Bodo saltans | 40% | 100% |
A0A422N932 | Trypanosoma rangeli | 24% | 100% |
A0A422NE52 | Trypanosoma rangeli | 48% | 100% |
A4H9E1 | Leishmania braziliensis | 23% | 100% |
A4HG29 | Leishmania braziliensis | 79% | 100% |
A4I351 | Leishmania infantum | 100% | 100% |
A4Q9E4 | Mus musculus | 27% | 99% |
E9ACW9 | Leishmania major | 94% | 100% |
E9ARH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9AZF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |