Structural Proteins, Uncharacterized
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4I7K6
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 13 |
GO:0007018 | microtubule-based movement | 3 | 13 |
GO:0009987 | cellular process | 1 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003774 | cytoskeletal motor activity | 1 | 13 |
GO:0003777 | microtubule motor activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005515 | protein binding | 2 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008017 | microtubule binding | 5 | 13 |
GO:0008092 | cytoskeletal protein binding | 3 | 13 |
GO:0015631 | tubulin binding | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.355 |
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.493 |
CLV_PCSK_FUR_1 | 214 | 218 | PF00082 | 0.450 |
CLV_PCSK_FUR_1 | 294 | 298 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 661 | 663 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 661 | 663 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 666 | 668 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.615 |
CLV_PCSK_PC7_1 | 123 | 129 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 662 | 668 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.391 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.472 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.394 |
DEG_SPOP_SBC_1 | 698 | 702 | PF00917 | 0.735 |
DOC_CYCLIN_RxL_1 | 120 | 130 | PF00134 | 0.387 |
DOC_MAPK_gen_1 | 221 | 231 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 455 | 463 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 686 | 692 | PF00069 | 0.707 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.323 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 43 | 50 | PF00149 | 0.443 |
DOC_PP1_RVXF_1 | 456 | 463 | PF00149 | 0.603 |
DOC_PP1_RVXF_1 | 665 | 672 | PF00149 | 0.618 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.472 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.445 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.785 |
LIG_14-3-3_CanoR_1 | 133 | 140 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 186 | 196 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 25 | 34 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 322 | 330 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 687 | 691 | PF00244 | 0.738 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BIR_III_4 | 451 | 455 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.323 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 472 | 480 | PF00928 | 0.352 |
LIG_deltaCOP1_diTrp_1 | 589 | 595 | PF00928 | 0.336 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.323 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.588 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.377 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.547 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.327 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.650 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.450 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.370 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.553 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.516 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.467 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.506 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.611 |
LIG_Integrin_isoDGR_2 | 499 | 501 | PF01839 | 0.394 |
LIG_LIR_Apic_2 | 107 | 112 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 320 | 331 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 199 | 203 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 578 | 583 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 677 | 681 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.340 |
LIG_PCNA_PIPBox_1 | 119 | 128 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 119 | 133 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 297 | 311 | PF02747 | 0.450 |
LIG_Pex14_1 | 590 | 594 | PF04695 | 0.343 |
LIG_Pex14_2 | 591 | 595 | PF04695 | 0.418 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.450 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.524 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.339 |
LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 471 | 474 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.354 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.632 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.662 |
LIG_SUMO_SIM_anti_2 | 81 | 87 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.427 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.556 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.541 |
LIG_UBA3_1 | 233 | 238 | PF00899 | 0.297 |
LIG_UBA3_1 | 416 | 422 | PF00899 | 0.473 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.258 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.394 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.467 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.666 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.378 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.387 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.362 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.388 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.533 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.433 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.513 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.511 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.364 |
MOD_Cter_Amidation | 499 | 502 | PF01082 | 0.440 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.440 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.427 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.649 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.710 |
MOD_GlcNHglycan | 670 | 674 | PF01048 | 0.607 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.383 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.381 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.459 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.448 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.421 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.323 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.450 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.534 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.394 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.720 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.434 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.336 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.519 |
MOD_N-GLC_2 | 575 | 577 | PF02516 | 0.541 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.422 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.475 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.654 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.473 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.499 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.572 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.439 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.472 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.411 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.582 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.370 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.535 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.450 |
MOD_PKA_1 | 247 | 253 | PF00069 | 0.450 |
MOD_PKA_1 | 686 | 692 | PF00069 | 0.728 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.419 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.418 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.433 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.549 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.560 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.430 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.519 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.733 |
MOD_PKB_1 | 23 | 31 | PF00069 | 0.481 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.450 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.384 |
MOD_Plk_2-3 | 344 | 350 | PF00069 | 0.450 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.323 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.431 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.394 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.458 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.189 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.340 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.323 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.299 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.609 |
MOD_Plk_4 | 709 | 715 | PF00069 | 0.640 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.472 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.724 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.712 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.784 |
TRG_AP2beta_CARGO_1 | 124 | 133 | PF09066 | 0.394 |
TRG_DiLeu_BaEn_1 | 376 | 381 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 81 | 86 | PF01217 | 0.370 |
TRG_DiLeu_BaEn_3 | 394 | 400 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 659 | 664 | PF01217 | 0.537 |
TRG_DiLeu_LyEn_5 | 376 | 381 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 681 | 684 | PF00928 | 0.607 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 660 | 663 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 667 | 669 | PF00400 | 0.547 |
TRG_NES_CRM1_1 | 414 | 429 | PF08389 | 0.423 |
TRG_NLS_MonoExtC_3 | 659 | 665 | PF00514 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 127 | 132 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 613 | 618 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 661 | 665 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2F2 | Leptomonas seymouri | 69% | 97% |
A0A0S4IK37 | Bodo saltans | 41% | 100% |
A0A0S4INH0 | Bodo saltans | 40% | 100% |
A0A1X0P6P1 | Trypanosomatidae | 46% | 100% |
A0A3S7X544 | Leishmania donovani | 100% | 100% |
A0A422N1G2 | Trypanosoma rangeli | 45% | 100% |
A4HK22 | Leishmania braziliensis | 86% | 100% |
D0A0B1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B2G3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q5P3 | Leishmania major | 95% | 100% |
V5C1Q9 | Trypanosoma cruzi | 46% | 100% |