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: A4H5M5
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_NRD_NRD_1 | 357 | 359 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.444 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.872 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.841 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.872 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.841 |
CLV_PCSK_PC1ET2_1 | 619 | 621 | PF00082 | 0.702 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.780 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.636 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.850 |
DEG_SPOP_SBC_1 | 476 | 480 | PF00917 | 0.482 |
DOC_CYCLIN_yClb1_LxF_4 | 256 | 261 | PF00134 | 0.306 |
DOC_MAPK_HePTP_8 | 556 | 568 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.755 |
DOC_MAPK_MEF2A_6 | 559 | 568 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 643 | 651 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 236 | 242 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 256 | 262 | PF00149 | 0.249 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.796 |
DOC_PP2B_LxvP_1 | 566 | 569 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.822 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.695 |
DOC_USP7_MATH_2 | 21 | 27 | PF00917 | 0.649 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.846 |
LIG_14-3-3_CanoR_1 | 422 | 432 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 457 | 464 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 47 | 53 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 527 | 535 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 620 | 628 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 643 | 651 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.824 |
LIG_APCC_ABBA_1 | 562 | 567 | PF00400 | 0.524 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.562 |
LIG_BRCT_BRCA1_1 | 504 | 508 | PF00533 | 0.446 |
LIG_Clathr_ClatBox_1 | 657 | 661 | PF01394 | 0.329 |
LIG_CtBP_PxDLS_1 | 659 | 663 | PF00389 | 0.511 |
LIG_EH1_1 | 142 | 150 | PF00400 | 0.530 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.530 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.630 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.636 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.530 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.302 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.645 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.681 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.488 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.491 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.450 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.672 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.508 |
LIG_FHA_2 | 621 | 627 | PF00498 | 0.323 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.621 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.433 |
LIG_HP1_1 | 322 | 326 | PF01393 | 0.476 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 650 | 659 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 650 | 654 | PF02991 | 0.492 |
LIG_PDZ_Class_1 | 667 | 672 | PF00595 | 0.445 |
LIG_Pex14_1 | 257 | 261 | PF04695 | 0.483 |
LIG_PTB_Apo_2 | 211 | 218 | PF02174 | 0.530 |
LIG_SH2_GRB2like | 212 | 215 | PF00017 | 0.530 |
LIG_SH2_GRB2like | 653 | 656 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 212 | 215 | PF00017 | 0.530 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.530 |
LIG_SH2_SRC | 212 | 215 | PF00017 | 0.530 |
LIG_SH2_SRC | 535 | 538 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.478 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.774 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.632 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.729 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.421 |
LIG_Sin3_3 | 222 | 229 | PF02671 | 0.602 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.609 |
LIG_SUMO_SIM_par_1 | 145 | 151 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 204 | 211 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 600 | 606 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 658 | 664 | PF11976 | 0.349 |
LIG_TRAF2_1 | 623 | 626 | PF00917 | 0.333 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.673 |
LIG_WRC_WIRS_1 | 113 | 118 | PF05994 | 0.702 |
LIG_WW_1 | 37 | 40 | PF00397 | 0.578 |
MOD_CDC14_SPxK_1 | 446 | 449 | PF00782 | 0.602 |
MOD_CDK_SPxK_1 | 443 | 449 | PF00069 | 0.603 |
MOD_CDK_SPxxK_3 | 5 | 12 | PF00069 | 0.580 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.392 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.246 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.739 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.595 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.535 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.543 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.734 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.557 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.774 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.636 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.411 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.747 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.571 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.714 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.610 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.578 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.549 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.616 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.375 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.741 |
MOD_Cter_Amidation | 427 | 430 | PF01082 | 0.624 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.530 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.343 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.794 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.837 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.809 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.644 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.654 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.651 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.582 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.409 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.779 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.748 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.564 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.572 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.597 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.583 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.687 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.811 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.704 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.655 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.709 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.741 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.614 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.628 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.621 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.843 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.527 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.704 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.678 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.623 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.490 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.759 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.747 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.608 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.365 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.483 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.530 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.799 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.707 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.865 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.851 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.601 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.704 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.556 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.608 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.613 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.587 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.622 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.747 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.644 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.492 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.411 |
MOD_PKB_1 | 117 | 125 | PF00069 | 0.673 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.577 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.663 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.530 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.799 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.420 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.344 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.779 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.611 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.603 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.578 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.791 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.519 |
MOD_SUMO_rev_2 | 19 | 27 | PF00179 | 0.805 |
MOD_SUMO_rev_2 | 330 | 335 | PF00179 | 0.595 |
MOD_SUMO_rev_2 | 378 | 384 | PF00179 | 0.645 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.465 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.542 |
TRG_NES_CRM1_1 | 23 | 35 | PF08389 | 0.544 |
TRG_NLS_MonoCore_2 | 355 | 360 | PF00514 | 0.609 |
TRG_NLS_MonoExtC_3 | 355 | 360 | PF00514 | 0.609 |
TRG_NLS_MonoExtN_4 | 353 | 360 | PF00514 | 0.765 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQM3 | Leishmania donovani | 62% | 90% |
A4HTW2 | Leishmania infantum | 62% | 90% |
E9AMP9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 93% |
Q4QHX6 | Leishmania major | 60% | 91% |