Transporters, 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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HTW2
Term | Name | Level | Count |
---|---|---|---|
GO:0032879 | regulation of localization | 3 | 6 |
GO:0034762 | regulation of transmembrane transport | 4 | 6 |
GO:0034765 | regulation of monoatomic ion transmembrane transport | 5 | 6 |
GO:0043269 | regulation of monoatomic ion transport | 5 | 6 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050794 | regulation of cellular process | 3 | 6 |
GO:0051049 | regulation of transport | 4 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0006812 | monoatomic cation transport | 5 | 1 |
GO:0006813 | potassium ion transport | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0030001 | metal ion transport | 6 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0071805 | potassium ion transmembrane transport | 6 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 1 |
GO:0098657 | import into cell | 4 | 1 |
GO:0098659 | inorganic cation import across plasma membrane | 5 | 1 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 1 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 1 |
GO:0098739 | import across plasma membrane | 3 | 1 |
GO:0099587 | inorganic ion import across plasma membrane | 4 | 1 |
GO:1990573 | potassium ion import across plasma membrane | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 6 |
GO:0005216 | monoatomic ion channel activity | 4 | 6 |
GO:0005242 | inward rectifier potassium channel activity | 7 | 6 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 6 |
GO:0005249 | voltage-gated potassium channel activity | 6 | 6 |
GO:0005261 | monoatomic cation channel activity | 5 | 6 |
GO:0005267 | potassium channel activity | 6 | 6 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 6 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 6 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 6 |
GO:0015267 | channel activity | 4 | 6 |
GO:0015276 | ligand-gated monoatomic ion channel activity | 5 | 6 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 6 |
GO:0022803 | passive transmembrane transporter activity | 3 | 6 |
GO:0022832 | voltage-gated channel activity | 6 | 6 |
GO:0022834 | ligand-gated channel activity | 6 | 6 |
GO:0022836 | gated channel activity | 5 | 6 |
GO:0022843 | voltage-gated monoatomic cation channel activity | 5 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 6 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 6 |
GO:0099094 | ligand-gated monoatomic cation channel activity | 6 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.753 |
CLV_PCSK_FUR_1 | 496 | 500 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.857 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.819 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.857 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.819 |
CLV_PCSK_PC1ET2_1 | 691 | 693 | PF00082 | 0.699 |
CLV_PCSK_PC7_1 | 395 | 401 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.804 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.570 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.843 |
DEG_SPOP_SBC_1 | 491 | 495 | PF00917 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 35 | PF00134 | 0.647 |
DOC_CYCLIN_yCln2_LP_2 | 618 | 624 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 610 | 618 | PF00069 | 0.486 |
DOC_MAPK_HePTP_8 | 628 | 640 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.717 |
DOC_MAPK_MEF2A_6 | 586 | 595 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 631 | 640 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 237 | 243 | PF00149 | 0.485 |
DOC_PP1_RVXF_1 | 257 | 263 | PF00149 | 0.479 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.765 |
DOC_PP2B_LxvP_1 | 638 | 641 | PF13499 | 0.524 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.815 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.780 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.632 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 106 | 114 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.839 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 426 | 436 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 448 | 457 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 599 | 607 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 613 | 619 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.801 |
LIG_APCC_ABBA_1 | 634 | 639 | PF00400 | 0.522 |
LIG_APCC_ABBA_1 | 710 | 715 | PF00400 | 0.485 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.569 |
LIG_BRCT_BRCA1_1 | 551 | 555 | PF00533 | 0.544 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.745 |
LIG_CtBP_PxDLS_1 | 731 | 735 | PF00389 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 256 | 262 | PF00928 | 0.432 |
LIG_EH1_1 | 143 | 151 | PF00400 | 0.530 |
LIG_eIF4E_1 | 144 | 150 | PF01652 | 0.530 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.575 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.630 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.636 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.524 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.475 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.784 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.678 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.524 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.513 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.431 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.633 |
LIG_GBD_Chelix_1 | 141 | 149 | PF00786 | 0.433 |
LIG_Integrin_isoDGR_2 | 104 | 106 | PF01839 | 0.374 |
LIG_KLC1_Yacidic_2 | 605 | 609 | PF13176 | 0.522 |
LIG_LIR_Apic_2 | 655 | 661 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 722 | 731 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 722 | 726 | PF02991 | 0.498 |
LIG_Pex14_1 | 258 | 262 | PF04695 | 0.477 |
LIG_PTB_Apo_2 | 212 | 219 | PF02174 | 0.530 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.452 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.530 |
LIG_SH2_GRB2like | 694 | 697 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 725 | 728 | PF00017 | 0.486 |
LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.530 |
LIG_SH2_SRC | 144 | 147 | PF00017 | 0.530 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 725 | 728 | PF00017 | 0.394 |
LIG_SH3_1 | 367 | 373 | PF00018 | 0.517 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.629 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.552 |
LIG_SH3_3 | 630 | 636 | PF00018 | 0.434 |
LIG_SH3_5 | 99 | 103 | PF00018 | 0.665 |
LIG_Sin3_3 | 223 | 230 | PF02671 | 0.601 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 205 | 212 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 672 | 678 | PF11976 | 0.475 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.552 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.452 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.706 |
MOD_CDC14_SPxK_1 | 421 | 424 | PF00782 | 0.704 |
MOD_CDC14_SPxK_1 | 632 | 635 | PF00782 | 0.504 |
MOD_CDK_SPK_2 | 418 | 423 | PF00069 | 0.676 |
MOD_CDK_SPK_2 | 506 | 511 | PF00069 | 0.768 |
MOD_CDK_SPxK_1 | 418 | 424 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 629 | 635 | PF00069 | 0.527 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.722 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.786 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.617 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.658 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.734 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.719 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.801 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.764 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.641 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.561 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.693 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.643 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.815 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.695 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.633 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.637 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.731 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.530 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.741 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.616 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.463 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.758 |
MOD_Cter_Amidation | 556 | 559 | PF01082 | 0.707 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.530 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.670 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.745 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.786 |
MOD_GlcNHglycan | 385 | 390 | PF01048 | 0.645 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.846 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.721 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.727 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.592 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.755 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.729 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.682 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.684 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.757 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.515 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.608 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.622 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.473 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.696 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.565 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.582 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.628 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.731 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.797 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.777 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.701 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.793 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.741 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.722 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.609 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.537 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.637 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.491 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.583 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.679 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.580 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.600 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.470 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.643 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.765 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.680 |
MOD_LATS_1 | 359 | 365 | PF00433 | 0.749 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.666 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.604 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.598 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.483 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.530 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.285 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.721 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.706 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.682 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.842 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.749 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.634 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.646 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.709 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.599 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.634 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.699 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.368 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.666 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.738 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.655 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.677 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.673 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.579 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.764 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.750 |
MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.586 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.663 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.249 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.530 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.723 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.664 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.448 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.743 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.816 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.766 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.783 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.727 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.639 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.504 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.643 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 19 | 27 | PF00179 | 0.722 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.703 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 496 | 499 | PF00400 | 0.633 |
TRG_NLS_MonoExtN_4 | 354 | 360 | PF00514 | 0.750 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQM3 | Leishmania donovani | 100% | 100% |
A4H5M5 | Leishmania braziliensis | 62% | 90% |
E9AMP9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
Q4QHX6 | Leishmania major | 88% | 99% |