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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AMP9
Term | Name | Level | Count |
---|---|---|---|
GO:0032879 | regulation of localization | 3 | 7 |
GO:0034762 | regulation of transmembrane transport | 4 | 7 |
GO:0034765 | regulation of monoatomic ion transmembrane transport | 5 | 7 |
GO:0043269 | regulation of monoatomic ion transport | 5 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051049 | regulation of transport | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
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 | 7 |
GO:0005216 | monoatomic ion channel activity | 4 | 7 |
GO:0005242 | inward rectifier potassium channel activity | 7 | 7 |
GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 7 |
GO:0005249 | voltage-gated potassium channel activity | 6 | 7 |
GO:0005261 | monoatomic cation channel activity | 5 | 7 |
GO:0005267 | potassium channel activity | 6 | 7 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 7 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 7 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 7 |
GO:0015267 | channel activity | 4 | 7 |
GO:0015276 | ligand-gated monoatomic ion channel activity | 5 | 7 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 7 |
GO:0022803 | passive transmembrane transporter activity | 3 | 7 |
GO:0022832 | voltage-gated channel activity | 6 | 7 |
GO:0022834 | ligand-gated channel activity | 6 | 7 |
GO:0022836 | gated channel activity | 5 | 7 |
GO:0022843 | voltage-gated monoatomic cation channel activity | 5 | 7 |
GO:0022857 | transmembrane transporter activity | 2 | 7 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 7 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 7 |
GO:0099094 | ligand-gated monoatomic cation channel activity | 6 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 673 | 675 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 649 | 657 | PF00400 | 0.470 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.736 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 600 | 606 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 592 | 600 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.675 |
DOC_PP1_RVXF_1 | 237 | 243 | PF00149 | 0.523 |
DOC_PP1_RVXF_1 | 257 | 263 | PF00149 | 0.518 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.721 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.837 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.751 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 366 | 373 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 463 | 468 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 495 | 503 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 581 | 589 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.700 |
LIG_APCC_ABBA_1 | 616 | 621 | PF00400 | 0.625 |
LIG_APCC_ABBA_1 | 692 | 697 | PF00400 | 0.594 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.637 |
LIG_deltaCOP1_diTrp_1 | 256 | 262 | PF00928 | 0.515 |
LIG_EH1_1 | 143 | 151 | PF00400 | 0.388 |
LIG_eIF4E_1 | 144 | 150 | PF01652 | 0.388 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.529 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.297 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.278 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.639 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.537 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.690 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.382 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.614 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.556 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.523 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.773 |
LIG_GBD_Chelix_1 | 141 | 149 | PF00786 | 0.327 |
LIG_KLC1_Yacidic_2 | 587 | 591 | PF13176 | 0.631 |
LIG_LIR_Apic_2 | 32 | 37 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 704 | 713 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 704 | 708 | PF02991 | 0.533 |
LIG_Pex14_1 | 258 | 262 | PF04695 | 0.516 |
LIG_Pex14_1 | 515 | 519 | PF04695 | 0.616 |
LIG_PTB_Apo_2 | 212 | 219 | PF02174 | 0.312 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.291 |
LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.312 |
LIG_SH2_GRB2like | 676 | 679 | PF00017 | 0.573 |
LIG_SH2_GRB2like | 707 | 710 | PF00017 | 0.517 |
LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.388 |
LIG_SH2_SRC | 144 | 147 | PF00017 | 0.388 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.312 |
LIG_SH2_SRC | 519 | 522 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.517 |
LIG_SH3_2 | 408 | 413 | PF14604 | 0.632 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.697 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.629 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.614 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.693 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.627 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.699 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.618 |
LIG_SH3_5 | 287 | 291 | PF00018 | 0.491 |
LIG_SH3_5 | 99 | 103 | PF00018 | 0.578 |
LIG_Sin3_3 | 223 | 230 | PF02671 | 0.381 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 205 | 212 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 654 | 660 | PF11976 | 0.574 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.291 |
LIG_ULM_U2AF65_1 | 412 | 417 | PF00076 | 0.550 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.563 |
LIG_WW_1 | 37 | 40 | PF00397 | 0.520 |
MOD_CDC14_SPxK_1 | 410 | 413 | PF00782 | 0.676 |
MOD_CDK_SPK_2 | 407 | 412 | PF00069 | 0.603 |
MOD_CDK_SPK_2 | 458 | 463 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 407 | 413 | PF00069 | 0.672 |
MOD_CDK_SPxxK_3 | 488 | 495 | PF00069 | 0.581 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.352 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.626 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.526 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.726 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.592 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.657 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.760 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.568 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.532 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.538 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.550 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.648 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.512 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.684 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.425 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.626 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.376 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.634 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.411 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.606 |
MOD_Cter_Amidation | 437 | 440 | PF01082 | 0.553 |
MOD_Cter_Amidation | 479 | 482 | PF01082 | 0.592 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.473 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.683 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.514 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.518 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.675 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.719 |
MOD_GlcNHglycan | 382 | 387 | PF01048 | 0.594 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.821 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.828 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.766 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.621 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.614 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.593 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.607 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.572 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.456 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.454 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.616 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.537 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.358 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.766 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.636 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.689 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.644 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.751 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.565 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.589 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.552 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.618 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.620 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.689 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.521 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.536 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.436 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.460 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.586 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.620 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.578 |
MOD_LATS_1 | 359 | 365 | PF00433 | 0.645 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.389 |
MOD_N-GLC_1 | 508 | 513 | PF02516 | 0.629 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.522 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.342 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.312 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.378 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.648 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.672 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.668 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.735 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.773 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.600 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.503 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.532 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.444 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.525 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.519 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.465 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.524 |
MOD_PK_1 | 463 | 469 | PF00069 | 0.514 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.588 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.573 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.652 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.518 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.428 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.518 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.672 |
MOD_PKB_1 | 118 | 126 | PF00069 | 0.529 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.451 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.521 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.650 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.675 |
MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.458 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.446 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.321 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.388 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.658 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.495 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.611 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.552 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.372 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.576 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.672 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.507 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.653 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.689 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.620 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.520 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.587 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.427 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.446 |
MOD_SUMO_rev_2 | 19 | 27 | PF00179 | 0.661 |
MOD_SUMO_rev_2 | 378 | 385 | PF00179 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.611 |
TRG_NLS_MonoExtN_4 | 354 | 360 | PF00514 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NMR1 | Trypanosomatidae | 40% | 100% |
A0A3S7WQM3 | Leishmania donovani | 83% | 98% |
A4H5M5 | Leishmania braziliensis | 59% | 92% |
A4HTW2 | Leishmania infantum | 83% | 98% |
Q4QHX6 | Leishmania major | 82% | 100% |