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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AQU0
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0007165 | signal transduction | 2 | 10 |
GO:0007186 | G protein-coupled receptor signaling pathway | 3 | 10 |
GO:0007205 | protein kinase C-activating G protein-coupled receptor signaling pathway | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0050789 | regulation of biological process | 2 | 10 |
GO:0050794 | regulation of cellular process | 3 | 10 |
GO:0065007 | biological regulation | 1 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004143 | diacylglycerol kinase activity | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.683 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.701 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 210 | 216 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.774 |
DEG_APCC_DBOX_1 | 517 | 525 | PF00400 | 0.388 |
DEG_COP1_1 | 100 | 108 | PF00400 | 0.756 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.714 |
DEG_SCF_FBW7_1 | 586 | 591 | PF00400 | 0.408 |
DEG_SCF_TRCP1_1 | 155 | 161 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 322 | 326 | PF00917 | 0.414 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 410 | 414 | PF00917 | 0.463 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.647 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.291 |
DOC_CKS1_1 | 652 | 657 | PF01111 | 0.485 |
DOC_CYCLIN_RxL_1 | 547 | 555 | PF00134 | 0.485 |
DOC_MAPK_DCC_7 | 364 | 374 | PF00069 | 0.495 |
DOC_MAPK_DCC_7 | 506 | 516 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 505 | 516 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 509 | 516 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 538 | 545 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 688 | 695 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.401 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.764 |
DOC_USP7_UBL2_3 | 505 | 509 | PF12436 | 0.429 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 651 | 656 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 499 | 503 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 577 | 582 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 688 | 692 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 722 | 729 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.696 |
LIG_AP2alpha_1 | 319 | 323 | PF02296 | 0.194 |
LIG_APCC_ABBA_1 | 67 | 72 | PF00400 | 0.518 |
LIG_BIR_III_2 | 103 | 107 | PF00653 | 0.472 |
LIG_BIR_III_4 | 28 | 32 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.756 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.725 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.496 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.386 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.454 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.669 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.514 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.455 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.392 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.577 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.344 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.486 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 441 | 447 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 537 | 546 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 645 | 655 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 666 | 675 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 441 | 445 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 666 | 671 | PF02991 | 0.618 |
LIG_MYND_1 | 300 | 304 | PF01753 | 0.444 |
LIG_PCNA_yPIPBox_3 | 484 | 496 | PF02747 | 0.448 |
LIG_Pex14_2 | 319 | 323 | PF04695 | 0.444 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.478 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.371 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.310 |
LIG_SH2_CRK | 576 | 580 | PF00017 | 0.444 |
LIG_SH2_CRK | 628 | 632 | PF00017 | 0.444 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.587 |
LIG_SH2_GRB2like | 313 | 316 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 677 | 681 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.533 |
LIG_SH3_1 | 220 | 226 | PF00018 | 0.291 |
LIG_SH3_2 | 109 | 114 | PF14604 | 0.472 |
LIG_SH3_2 | 396 | 401 | PF14604 | 0.589 |
LIG_SH3_2 | 566 | 571 | PF14604 | 0.408 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.691 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.699 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.465 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.411 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.654 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.387 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.444 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.735 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.422 |
LIG_SH3_CIN85_PxpxPR_1 | 603 | 608 | PF14604 | 0.422 |
LIG_SUMO_SIM_par_1 | 608 | 614 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 97 | 103 | PF11976 | 0.774 |
LIG_SxIP_EBH_1 | 585 | 599 | PF03271 | 0.194 |
LIG_TYR_ITIM | 457 | 462 | PF00017 | 0.344 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.444 |
LIG_TYR_ITIM | 626 | 631 | PF00017 | 0.444 |
LIG_WW_3 | 79 | 83 | PF00397 | 0.609 |
MOD_CDK_SPK_2 | 603 | 608 | PF00069 | 0.369 |
MOD_CDK_SPxK_1 | 108 | 114 | PF00069 | 0.579 |
MOD_CDK_SPxK_1 | 219 | 225 | PF00069 | 0.369 |
MOD_CDK_SPxxK_3 | 601 | 608 | PF00069 | 0.291 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.443 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.314 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.692 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.612 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.644 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.366 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.420 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.463 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.530 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.601 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.687 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.539 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.709 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.757 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.379 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.263 |
MOD_GlcNHglycan | 279 | 283 | PF01048 | 0.423 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.583 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.685 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.498 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.429 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.730 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.466 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.485 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.611 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.560 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.517 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.596 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.616 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.452 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.818 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.508 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.429 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.407 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.697 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.368 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.779 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.389 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.538 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.564 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.778 |
MOD_LATS_1 | 575 | 581 | PF00433 | 0.408 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.821 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.697 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.331 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.485 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.635 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.380 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.344 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.425 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.422 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.252 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.194 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.700 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.567 |
MOD_PK_1 | 724 | 730 | PF00069 | 0.552 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.344 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.397 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.522 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.669 |
MOD_PKB_1 | 276 | 284 | PF00069 | 0.194 |
MOD_PKB_1 | 722 | 730 | PF00069 | 0.539 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.491 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.485 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.482 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.552 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.588 |
MOD_Plk_2-3 | 94 | 100 | PF00069 | 0.556 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.344 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.344 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.482 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.739 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.498 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.476 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.266 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.798 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.735 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.649 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.478 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.630 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.706 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.435 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.280 |
MOD_ProDKin_1 | 651 | 657 | PF00069 | 0.454 |
MOD_SUMO_for_1 | 675 | 678 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 3 | 8 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_2 | 645 | 651 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_3 | 259 | 265 | PF01217 | 0.194 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.581 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 721 | 724 | PF00400 | 0.435 |
TRG_NLS_MonoExtN_4 | 569 | 574 | PF00514 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRI7 | Leptomonas seymouri | 50% | 97% |
A0A3Q8IAN3 | Leishmania donovani | 86% | 100% |
A0A3R7MJ80 | Trypanosoma rangeli | 33% | 100% |
A4H8Q7 | Leishmania braziliensis | 69% | 96% |
A4HX26 | Leishmania infantum | 86% | 100% |
C9ZVX0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4QEN8 | Leishmania major | 85% | 99% |
V5DJ39 | Trypanosoma cruzi | 33% | 100% |