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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A0A3S7WVK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0036211 | protein modification process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004672 | protein kinase activity | 3 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0016301 | kinase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.823 |
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.801 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.740 |
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.817 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.801 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.719 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.817 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.813 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.735 |
CLV_Separin_Metazoa | 759 | 763 | PF03568 | 0.750 |
DEG_APCC_DBOX_1 | 597 | 605 | PF00400 | 0.735 |
DEG_APCC_DBOX_1 | 710 | 718 | PF00400 | 0.602 |
DEG_SCF_FBW7_1 | 256 | 262 | PF00400 | 0.724 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.846 |
DOC_CDC14_PxL_1 | 154 | 162 | PF14671 | 0.606 |
DOC_CKS1_1 | 176 | 181 | PF01111 | 0.786 |
DOC_CKS1_1 | 256 | 261 | PF01111 | 0.724 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.697 |
DOC_CYCLIN_RxL_1 | 367 | 377 | PF00134 | 0.766 |
DOC_CYCLIN_RxL_1 | 684 | 695 | PF00134 | 0.763 |
DOC_CYCLIN_RxL_1 | 700 | 709 | PF00134 | 0.739 |
DOC_CYCLIN_RxL_1 | 710 | 718 | PF00134 | 0.571 |
DOC_CYCLIN_yClb3_PxF_3 | 179 | 187 | PF00134 | 0.661 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 338 | 347 | PF00134 | 0.683 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 24 | 27 | PF00134 | 0.782 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 790 | 798 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 762 | 769 | PF00069 | 0.675 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.752 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.722 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.764 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.783 |
DOC_PP2B_LxvP_1 | 758 | 761 | PF13499 | 0.690 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.729 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.701 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 788 | 792 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 831 | 835 | PF00917 | 0.730 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.841 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 814 | 819 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 451 | 455 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 526 | 531 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 590 | 600 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 792 | 797 | PF00244 | 0.718 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.777 |
LIG_Actin_WH2_2 | 738 | 754 | PF00022 | 0.524 |
LIG_AP2alpha_1 | 798 | 802 | PF02296 | 0.705 |
LIG_BIR_III_2 | 699 | 703 | PF00653 | 0.567 |
LIG_BIR_III_4 | 464 | 468 | PF00653 | 0.670 |
LIG_BIR_III_4 | 572 | 576 | PF00653 | 0.803 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.769 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 528 | 532 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 663 | 667 | PF00533 | 0.769 |
LIG_CaM_IQ_9 | 738 | 754 | PF13499 | 0.699 |
LIG_Clathr_ClatBox_1 | 714 | 718 | PF01394 | 0.731 |
LIG_CtBP_PxDLS_1 | 560 | 566 | PF00389 | 0.736 |
LIG_deltaCOP1_diTrp_1 | 474 | 482 | PF00928 | 0.710 |
LIG_deltaCOP1_diTrp_1 | 661 | 667 | PF00928 | 0.764 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.692 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.723 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.602 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.770 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.754 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.408 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.658 |
LIG_FHA_1 | 764 | 770 | PF00498 | 0.579 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.639 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.737 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.741 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.779 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.742 |
LIG_LIR_Gen_1 | 729 | 739 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 29 | 33 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 599 | 603 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 729 | 734 | PF02991 | 0.714 |
LIG_LIR_Nem_3 | 800 | 805 | PF02991 | 0.702 |
LIG_MYND_1 | 130 | 134 | PF01753 | 0.701 |
LIG_NRBOX | 716 | 722 | PF00104 | 0.727 |
LIG_PCNA_yPIPBox_3 | 395 | 405 | PF02747 | 0.746 |
LIG_Pex14_1 | 476 | 480 | PF04695 | 0.715 |
LIG_Pex14_1 | 663 | 667 | PF04695 | 0.769 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.660 |
LIG_Pex14_2 | 798 | 802 | PF04695 | 0.705 |
LIG_PTB_Apo_2 | 474 | 481 | PF02174 | 0.714 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.771 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.595 |
LIG_SH2_STAT3 | 784 | 787 | PF00017 | 0.726 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.814 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 851 | 854 | PF00017 | 0.764 |
LIG_SH3_1 | 102 | 108 | PF00018 | 0.628 |
LIG_SH3_1 | 187 | 193 | PF00018 | 0.819 |
LIG_SH3_2 | 130 | 135 | PF14604 | 0.700 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.628 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.713 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.810 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.618 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.743 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.810 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.773 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.758 |
LIG_SUMO_SIM_anti_2 | 35 | 43 | PF11976 | 0.635 |
LIG_SUMO_SIM_anti_2 | 599 | 606 | PF11976 | 0.603 |
LIG_SUMO_SIM_anti_2 | 764 | 769 | PF11976 | 0.729 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 381 | 386 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 713 | 718 | PF11976 | 0.728 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.804 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.720 |
LIG_TRAF2_1 | 783 | 786 | PF00917 | 0.769 |
LIG_TRAF2_2 | 540 | 545 | PF00917 | 0.778 |
LIG_WW_3 | 132 | 136 | PF00397 | 0.745 |
MOD_CDK_SPK_2 | 211 | 216 | PF00069 | 0.807 |
MOD_CDK_SPK_2 | 509 | 514 | PF00069 | 0.613 |
MOD_CDK_SPxK_1 | 117 | 123 | PF00069 | 0.843 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.684 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.823 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.720 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.629 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.633 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.579 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.773 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.821 |
MOD_Cter_Amidation | 449 | 452 | PF01082 | 0.706 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.738 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.668 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.787 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.575 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.484 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.578 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.731 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.694 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.647 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.590 |
MOD_GlcNHglycan | 572 | 576 | PF01048 | 0.698 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.614 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.683 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.517 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.747 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.828 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.661 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.634 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.699 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.674 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.754 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.792 |
MOD_LATS_1 | 208 | 214 | PF00433 | 0.624 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.671 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.707 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.725 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.731 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.586 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.568 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.439 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.685 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.697 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.676 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.636 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.760 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.744 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.747 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.535 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.555 |
MOD_NEK2_2 | 390 | 395 | PF00069 | 0.591 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.843 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.835 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.741 |
MOD_PIKK_1 | 746 | 752 | PF00454 | 0.697 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.782 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.720 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.650 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.722 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.718 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.783 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.719 |
MOD_PKB_1 | 790 | 798 | PF00069 | 0.719 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.741 |
MOD_Plk_1 | 763 | 769 | PF00069 | 0.695 |
MOD_Plk_1 | 778 | 784 | PF00069 | 0.536 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.674 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.479 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.771 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.650 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.843 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.830 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.655 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.809 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.723 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.702 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.701 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.597 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.788 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.743 |
MOD_ProDKin_1 | 814 | 820 | PF00069 | 0.695 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.771 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.689 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.769 |
TRG_DiLeu_BaEn_1 | 716 | 721 | PF01217 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 368 | 373 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.752 |
TRG_DiLeu_BaLyEn_6 | 710 | 715 | PF01217 | 0.737 |
TRG_DiLeu_BaLyEn_6 | 816 | 821 | PF01217 | 0.747 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.814 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.773 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.811 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.778 |
TRG_ER_diArg_1 | 710 | 713 | PF00400 | 0.737 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.805 |
TRG_Pf-PMV_PEXEL_1 | 370 | 374 | PF00026 | 0.762 |
TRG_Pf-PMV_PEXEL_1 | 452 | 457 | PF00026 | 0.852 |
TRG_Pf-PMV_PEXEL_1 | 679 | 683 | PF00026 | 0.705 |
TRG_Pf-PMV_PEXEL_1 | 713 | 718 | PF00026 | 0.730 |
TRG_Pf-PMV_PEXEL_1 | 746 | 750 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 775 | 779 | PF00026 | 0.723 |