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 |
Related structures:
AlphaFold database: A0A3Q8IG93
Term | Name | Level | Count |
---|---|---|---|
GO:0000079 | regulation of cyclin-dependent protein serine/threonine kinase activity | 6 | 7 |
GO:0001932 | regulation of protein phosphorylation | 7 | 7 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
GO:0031399 | regulation of protein modification process | 6 | 7 |
GO:0042325 | regulation of phosphorylation | 7 | 7 |
GO:0043549 | regulation of kinase activity | 5 | 7 |
GO:0045859 | regulation of protein kinase activity | 6 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 7 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 7 |
GO:0051246 | regulation of protein metabolic process | 5 | 7 |
GO:0051338 | regulation of transferase activity | 4 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 7 |
GO:0080090 | regulation of primary metabolic process | 4 | 7 |
GO:1904029 | regulation of cyclin-dependent protein kinase activity | 5 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0019899 | enzyme binding | 3 | 7 |
GO:0019900 | kinase binding | 4 | 7 |
GO:0019901 | protein kinase binding | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.712 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 607 | 613 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.795 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.714 |
CLV_Separin_Metazoa | 130 | 134 | PF03568 | 0.625 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.542 |
DEG_SCF_FBW7_1 | 336 | 342 | PF00400 | 0.735 |
DEG_SCF_FBW7_1 | 78 | 84 | PF00400 | 0.770 |
DEG_SPOP_SBC_1 | 581 | 585 | PF00917 | 0.591 |
DOC_CKS1_1 | 336 | 341 | PF01111 | 0.732 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.670 |
DOC_CYCLIN_yClb1_LxF_4 | 287 | 293 | PF00134 | 0.411 |
DOC_CYCLIN_yClb1_LxF_4 | 299 | 304 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 245 | 251 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 632 | 642 | PF00069 | 0.735 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 522 | 525 | PF13499 | 0.802 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.798 |
DOC_PP2B_PxIxI_1 | 204 | 210 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.458 |
DOC_SPAK_OSR1_1 | 112 | 116 | PF12202 | 0.475 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.503 |
DOC_USP7_MATH_2 | 339 | 345 | PF00917 | 0.826 |
DOC_USP7_UBL2_3 | 214 | 218 | PF12436 | 0.375 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 405 | 410 | PF00244 | 0.825 |
LIG_14-3-3_CanoR_1 | 478 | 487 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 586 | 595 | PF00244 | 0.801 |
LIG_14-3-3_CanoR_1 | 629 | 639 | PF00244 | 0.782 |
LIG_BIR_III_4 | 534 | 538 | PF00653 | 0.783 |
LIG_Clathr_ClatBox_1 | 506 | 510 | PF01394 | 0.757 |
LIG_EH1_1 | 291 | 299 | PF00400 | 0.563 |
LIG_eIF4E_1 | 249 | 255 | PF01652 | 0.499 |
LIG_EVH1_1 | 63 | 67 | PF00568 | 0.608 |
LIG_EVH1_1 | 649 | 653 | PF00568 | 0.800 |
LIG_FAT_LD_1 | 290 | 298 | PF03623 | 0.556 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.411 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.411 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.825 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.797 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.755 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.704 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.756 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.440 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.555 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.672 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.408 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.589 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.793 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.762 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.644 |
LIG_Integrin_RGD_1 | 512 | 514 | PF01839 | 0.718 |
LIG_LIR_Apic_2 | 110 | 116 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 220 | 224 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 310 | 315 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 275 | 282 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 291 | 298 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.290 |
LIG_MYND_1 | 61 | 65 | PF01753 | 0.736 |
LIG_NRBOX | 233 | 239 | PF00104 | 0.411 |
LIG_Pex14_2 | 113 | 117 | PF04695 | 0.559 |
LIG_PTB_Apo_2 | 270 | 277 | PF02174 | 0.353 |
LIG_PTB_Apo_2 | 297 | 304 | PF02174 | 0.477 |
LIG_PTB_Phospho_1 | 297 | 303 | PF10480 | 0.480 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.478 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.454 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 221 | 224 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.433 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.759 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.714 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.710 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.688 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.667 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.709 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.567 |
LIG_SUMO_SIM_par_1 | 504 | 511 | PF11976 | 0.732 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.550 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.731 |
LIG_TRFH_1 | 77 | 81 | PF08558 | 0.641 |
LIG_TYR_ITIM | 217 | 222 | PF00017 | 0.411 |
LIG_WW_2 | 64 | 67 | PF00397 | 0.627 |
MOD_CDC14_SPxK_1 | 387 | 390 | PF00782 | 0.705 |
MOD_CDK_SPK_2 | 159 | 164 | PF00069 | 0.751 |
MOD_CDK_SPxK_1 | 384 | 390 | PF00069 | 0.702 |
MOD_CDK_SPxK_1 | 605 | 611 | PF00069 | 0.696 |
MOD_CDK_SPxxK_3 | 605 | 612 | PF00069 | 0.700 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.785 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.718 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.309 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.488 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.723 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.781 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.798 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.689 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.813 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.697 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.690 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.693 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.621 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.611 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.678 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.411 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.548 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.786 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.697 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.642 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.566 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.731 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.750 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.399 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.683 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.822 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.486 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.693 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.709 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.715 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.576 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.772 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.783 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.727 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.710 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.830 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.766 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.539 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.745 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.790 |
MOD_GlcNHglycan | 634 | 638 | PF01048 | 0.813 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.671 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.674 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.777 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.621 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.610 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.478 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.411 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.611 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.640 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.700 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.558 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.815 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.717 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.737 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.728 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.596 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.810 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.691 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.549 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.722 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.681 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.731 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.757 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.701 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.804 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.699 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.584 |
MOD_N-GLC_2 | 570 | 572 | PF02516 | 0.723 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.411 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.722 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.680 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.775 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.411 |
MOD_NEK2_2 | 8 | 13 | PF00069 | 0.718 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.697 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.689 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.700 |
MOD_PK_1 | 405 | 411 | PF00069 | 0.824 |
MOD_PK_1 | 516 | 522 | PF00069 | 0.710 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.701 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.737 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.590 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.701 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.797 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.612 |
MOD_PKB_1 | 364 | 372 | PF00069 | 0.700 |
MOD_PKB_1 | 516 | 524 | PF00069 | 0.808 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.461 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.411 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.690 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.624 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.566 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.411 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.679 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.721 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.652 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.512 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.799 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.733 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.732 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.682 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.774 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.513 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.411 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.730 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.702 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.715 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.714 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.801 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.724 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.700 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.696 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.632 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 538 | 543 | PF01217 | 0.759 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.707 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.689 |
TRG_NES_CRM1_1 | 285 | 296 | PF08389 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 314 | 319 | PF00026 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0K2 | Leptomonas seymouri | 51% | 94% |
A4HDQ0 | Leishmania braziliensis | 79% | 100% |
A4I0Z6 | Leishmania infantum | 99% | 100% |
E9AX34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QAE2 | Leishmania major | 95% | 100% |