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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0020023 | kinetoplast | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WTB0
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.238 |
DEG_SCF_FBW7_1 | 289 | 295 | PF00400 | 0.473 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 337 | 349 | PF00134 | 0.652 |
DOC_MAPK_DCC_7 | 221 | 230 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 221 | 230 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 417 | 425 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 463 | 473 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.487 |
DOC_PP1_RVXF_1 | 231 | 238 | PF00149 | 0.490 |
DOC_PP1_RVXF_1 | 279 | 286 | PF00149 | 0.374 |
DOC_PP4_FxxP_1 | 341 | 344 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.661 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 47 | 56 | PF00244 | 0.747 |
LIG_Actin_WH2_2 | 262 | 280 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 72 | 89 | PF00022 | 0.567 |
LIG_BIR_III_2 | 349 | 353 | PF00653 | 0.578 |
LIG_BIR_III_4 | 448 | 452 | PF00653 | 0.553 |
LIG_BRCT_BRCA1_1 | 118 | 122 | PF00533 | 0.390 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.438 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.487 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.660 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.507 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.489 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 38 | 43 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 140 | 148 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 279 | 290 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 470 | 476 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.545 |
LIG_MLH1_MIPbox_1 | 118 | 122 | PF16413 | 0.390 |
LIG_MLH1_MIPbox_1 | 383 | 387 | PF16413 | 0.438 |
LIG_PDZ_Class_3 | 471 | 476 | PF00595 | 0.559 |
LIG_REV1ctd_RIR_1 | 118 | 128 | PF16727 | 0.503 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.469 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.398 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 90 | 93 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.680 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.433 |
LIG_SH3_2 | 145 | 150 | PF14604 | 0.491 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.535 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.433 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.544 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.543 |
LIG_SUMO_SIM_anti_2 | 318 | 325 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 343 | 349 | PF11976 | 0.673 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.574 |
LIG_TRFH_1 | 285 | 289 | PF08558 | 0.515 |
LIG_TYR_ITSM | 227 | 234 | PF00017 | 0.448 |
LIG_WW_3 | 146 | 150 | PF00397 | 0.433 |
MOD_CDK_SPK_2 | 9 | 14 | PF00069 | 0.460 |
MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.592 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.626 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.680 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.593 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.503 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.341 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.533 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.533 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.697 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.505 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.454 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.744 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.400 |
MOD_Cter_Amidation | 415 | 418 | PF01082 | 0.420 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.563 |
MOD_GlcNHglycan | 191 | 197 | PF01048 | 0.663 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.514 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.585 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.729 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.477 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.771 |
MOD_GlcNHglycan | 378 | 383 | PF01048 | 0.308 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.629 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.653 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.638 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.672 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.432 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.602 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.648 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.567 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.492 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.487 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.340 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.701 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.531 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.428 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.625 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.451 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.463 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.629 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.532 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.777 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.435 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.614 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.296 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.487 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.764 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.656 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.593 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.514 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.493 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.448 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.451 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.469 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.543 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.676 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.619 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.694 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.417 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.598 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.570 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.651 |
MOD_SUMO_rev_2 | 211 | 219 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 362 | 370 | PF00179 | 0.525 |
TRG_DiLeu_BaEn_1 | 319 | 324 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.680 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L8 | Leptomonas seymouri | 52% | 87% |
A0A1X0NNT6 | Trypanosomatidae | 40% | 100% |
A0A3R7R786 | Trypanosoma rangeli | 37% | 100% |
A4H7R7 | Leishmania braziliensis | 73% | 100% |
A4HW60 | Leishmania infantum | 100% | 100% |
C9ZSW3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9APW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4QFM0 | Leishmania major | 92% | 100% |
V5DC73 | Trypanosoma cruzi | 38% | 100% |