LeishMANIAdb
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Uncharacterized protein

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4HSR9_LEIIN
TriTrypDb:
LINF_060008100
Length:
855

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0030870 Mre11 complex 3 7
GO:0032991 protein-containing complex 1 7
GO:0140513 nuclear protein-containing complex 2 7
GO:0005737 cytoplasm 2 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4HSR9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HSR9

Function

Biological processes
Term Name Level Count
GO:0000075 cell cycle checkpoint signaling 4 7
GO:0000077 DNA damage checkpoint signaling 5 7
GO:0006139 nucleobase-containing compound metabolic process 3 7
GO:0006259 DNA metabolic process 4 7
GO:0006281 DNA repair 5 7
GO:0006302 double-strand break repair 6 7
GO:0006725 cellular aromatic compound metabolic process 3 7
GO:0006807 nitrogen compound metabolic process 2 7
GO:0006950 response to stress 2 7
GO:0006974 DNA damage response 4 7
GO:0007093 mitotic cell cycle checkpoint signaling 4 7
GO:0007095 mitotic G2 DNA damage checkpoint signaling 6 7
GO:0007165 signal transduction 2 7
GO:0007346 regulation of mitotic cell cycle 5 7
GO:0008152 metabolic process 1 7
GO:0009987 cellular process 1 7
GO:0010389 regulation of G2/M transition of mitotic cell cycle 7 7
GO:0010564 regulation of cell cycle process 5 7
GO:0010948 negative regulation of cell cycle process 6 7
GO:0010972 negative regulation of G2/M transition of mitotic cell cycle 8 7
GO:0022402 cell cycle process 2 7
GO:0031570 DNA integrity checkpoint signaling 5 7
GO:0033554 cellular response to stress 3 7
GO:0034641 cellular nitrogen compound metabolic process 3 7
GO:0035556 intracellular signal transduction 3 7
GO:0042770 signal transduction in response to DNA damage 4 7
GO:0043170 macromolecule metabolic process 3 7
GO:0044237 cellular metabolic process 2 7
GO:0044238 primary metabolic process 2 7
GO:0044260 obsolete cellular macromolecule metabolic process 3 7
GO:0044773 mitotic DNA damage checkpoint signaling 6 7
GO:0044774 mitotic DNA integrity checkpoint signaling 5 7
GO:0044818 mitotic G2/M transition checkpoint 5 7
GO:0045786 negative regulation of cell cycle 5 7
GO:0045930 negative regulation of mitotic cell cycle 6 7
GO:0046483 heterocycle metabolic process 3 7
GO:0048519 negative regulation of biological process 3 7
GO:0048523 negative regulation of cellular process 4 7
GO:0050789 regulation of biological process 2 7
GO:0050794 regulation of cellular process 3 7
GO:0050896 response to stimulus 1 7
GO:0051716 cellular response to stimulus 2 7
GO:0051726 regulation of cell cycle 4 7
GO:0065007 biological regulation 1 7
GO:0071704 organic substance metabolic process 2 7
GO:0090304 nucleic acid metabolic process 4 7
GO:1901360 organic cyclic compound metabolic process 3 7
GO:1901987 regulation of cell cycle phase transition 6 7
GO:1901988 negative regulation of cell cycle phase transition 7 7
GO:1901990 regulation of mitotic cell cycle phase transition 6 7
GO:1901991 negative regulation of mitotic cell cycle phase transition 7 7
GO:1902749 regulation of cell cycle G2/M phase transition 7 7
GO:1902750 negative regulation of cell cycle G2/M phase transition 8 7
GO:1903047 mitotic cell cycle process 3 7
GO:0000724 double-strand break repair via homologous recombination 7 1
GO:0000725 recombinational repair 6 1
GO:0006310 DNA recombination 5 1
GO:0006996 organelle organization 4 1
GO:0016043 cellular component organization 3 1
GO:0032392 DNA geometric change 7 1
GO:0032508 DNA duplex unwinding 8 1
GO:0051276 chromosome organization 5 1
GO:0071103 DNA conformation change 6 1
GO:0071840 cellular component organization or biogenesis 2 1
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 1
GO:0003677 DNA binding 4 1
GO:0003684 damaged DNA binding 5 1
GO:0005488 binding 1 1
GO:0097159 organic cyclic compound binding 2 1
GO:1901363 heterocyclic compound binding 2 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 195 199 PF00656 0.387
CLV_C14_Caspase3-7 239 243 PF00656 0.653
CLV_C14_Caspase3-7 430 434 PF00656 0.465
CLV_C14_Caspase3-7 610 614 PF00656 0.787
CLV_C14_Caspase3-7 66 70 PF00656 0.476
CLV_C14_Caspase3-7 839 843 PF00656 0.566
CLV_NRD_NRD_1 133 135 PF00675 0.742
CLV_NRD_NRD_1 408 410 PF00675 0.598
CLV_NRD_NRD_1 574 576 PF00675 0.710
CLV_NRD_NRD_1 605 607 PF00675 0.731
CLV_NRD_NRD_1 708 710 PF00675 0.696
CLV_NRD_NRD_1 766 768 PF00675 0.717
CLV_NRD_NRD_1 772 774 PF00675 0.724
CLV_NRD_NRD_1 803 805 PF00675 0.626
CLV_PCSK_FUR_1 706 710 PF00082 0.723
CLV_PCSK_KEX2_1 135 137 PF00082 0.745
CLV_PCSK_KEX2_1 408 410 PF00082 0.593
CLV_PCSK_KEX2_1 574 576 PF00082 0.710
CLV_PCSK_KEX2_1 605 607 PF00082 0.714
CLV_PCSK_KEX2_1 708 710 PF00082 0.696
CLV_PCSK_KEX2_1 765 767 PF00082 0.715
CLV_PCSK_KEX2_1 772 774 PF00082 0.724
CLV_PCSK_KEX2_1 803 805 PF00082 0.626
CLV_PCSK_PC1ET2_1 135 137 PF00082 0.745
CLV_PCSK_PC7_1 799 805 PF00082 0.634
CLV_PCSK_SKI1_1 348 352 PF00082 0.495
CLV_PCSK_SKI1_1 409 413 PF00082 0.595
CLV_PCSK_SKI1_1 461 465 PF00082 0.640
CLV_PCSK_SKI1_1 476 480 PF00082 0.335
CLV_PCSK_SKI1_1 55 59 PF00082 0.557
CLV_PCSK_SKI1_1 620 624 PF00082 0.803
CLV_PCSK_SKI1_1 683 687 PF00082 0.679
CLV_PCSK_SKI1_1 690 694 PF00082 0.663
DEG_APCC_DBOX_1 347 355 PF00400 0.561
DEG_APCC_DBOX_1 408 416 PF00400 0.375
DEG_APCC_DBOX_1 460 468 PF00400 0.626
DEG_COP1_1 714 723 PF00400 0.793
DEG_Nend_Nbox_1 1 3 PF02207 0.437
DEG_SCF_FBW7_1 254 261 PF00400 0.788
DEG_SPOP_SBC_1 455 459 PF00917 0.640
DOC_CKS1_1 314 319 PF01111 0.546
DOC_CKS1_1 550 555 PF01111 0.548
DOC_CYCLIN_RxL_1 405 416 PF00134 0.594
DOC_CYCLIN_yCln2_LP_2 449 455 PF00134 0.624
DOC_CYCLIN_yCln2_LP_2 649 655 PF00134 0.665
DOC_MAPK_DCC_7 58 67 PF00069 0.424
DOC_MAPK_gen_1 21 31 PF00069 0.586
DOC_MAPK_gen_1 282 292 PF00069 0.528
DOC_MAPK_gen_1 473 481 PF00069 0.585
DOC_MAPK_gen_1 803 811 PF00069 0.586
DOC_MAPK_MEF2A_6 145 154 PF00069 0.609
DOC_MAPK_MEF2A_6 326 333 PF00069 0.526
DOC_MAPK_MEF2A_6 39 48 PF00069 0.497
DOC_PP1_RVXF_1 182 188 PF00149 0.455
DOC_PP1_RVXF_1 436 442 PF00149 0.606
DOC_PP2B_LxvP_1 449 452 PF13499 0.599
DOC_PP2B_LxvP_1 521 524 PF13499 0.578
DOC_PP2B_LxvP_1 693 696 PF13499 0.660
DOC_PP4_FxxP_1 618 621 PF00568 0.807
DOC_USP7_MATH_1 278 282 PF00917 0.580
DOC_USP7_MATH_1 334 338 PF00917 0.549
DOC_USP7_MATH_1 342 346 PF00917 0.424
DOC_USP7_MATH_1 358 362 PF00917 0.635
DOC_USP7_MATH_1 386 390 PF00917 0.686
DOC_USP7_MATH_1 394 398 PF00917 0.499
DOC_USP7_MATH_1 455 459 PF00917 0.564
DOC_USP7_MATH_1 466 470 PF00917 0.476
DOC_USP7_MATH_1 548 552 PF00917 0.603
DOC_USP7_MATH_1 637 641 PF00917 0.731
DOC_USP7_MATH_1 669 673 PF00917 0.744
DOC_USP7_MATH_1 840 844 PF00917 0.628
DOC_USP7_UBL2_3 686 690 PF12436 0.675
DOC_WW_Pin1_4 107 112 PF00397 0.517
DOC_WW_Pin1_4 254 259 PF00397 0.683
DOC_WW_Pin1_4 260 265 PF00397 0.691
DOC_WW_Pin1_4 313 318 PF00397 0.445
DOC_WW_Pin1_4 325 330 PF00397 0.514
DOC_WW_Pin1_4 549 554 PF00397 0.531
DOC_WW_Pin1_4 6 11 PF00397 0.603
DOC_WW_Pin1_4 784 789 PF00397 0.695
DOC_WW_Pin1_4 90 95 PF00397 0.797
LIG_14-3-3_CanoR_1 138 148 PF00244 0.725
LIG_14-3-3_CanoR_1 166 170 PF00244 0.530
LIG_14-3-3_CanoR_1 285 291 PF00244 0.515
LIG_14-3-3_CanoR_1 498 504 PF00244 0.590
LIG_14-3-3_CanoR_1 574 582 PF00244 0.701
LIG_Actin_WH2_2 169 186 PF00022 0.474
LIG_APCC_ABBA_1 3 8 PF00400 0.489
LIG_APCC_ABBA_1 478 483 PF00400 0.475
LIG_BIR_III_2 577 581 PF00653 0.799
LIG_BRCT_BRCA1_1 842 846 PF00533 0.682
LIG_Clathr_ClatBox_1 185 189 PF01394 0.464
LIG_Clathr_ClatBox_1 699 703 PF01394 0.728
LIG_CtBP_PxDLS_1 245 251 PF00389 0.627
LIG_deltaCOP1_diTrp_1 613 618 PF00928 0.807
LIG_EVH1_1 521 525 PF00568 0.594
LIG_EVH1_1 655 659 PF00568 0.657
LIG_FHA_1 153 159 PF00498 0.537
LIG_FHA_1 171 177 PF00498 0.548
LIG_FHA_1 221 227 PF00498 0.756
LIG_FHA_1 293 299 PF00498 0.459
LIG_FHA_1 300 306 PF00498 0.455
LIG_FHA_1 41 47 PF00498 0.483
LIG_FHA_1 414 420 PF00498 0.564
LIG_FHA_1 482 488 PF00498 0.578
LIG_FHA_1 545 551 PF00498 0.642
LIG_FHA_1 643 649 PF00498 0.623
LIG_FHA_1 715 721 PF00498 0.743
LIG_FHA_1 73 79 PF00498 0.583
LIG_FHA_2 508 514 PF00498 0.527
LIG_FHA_2 533 539 PF00498 0.569
LIG_FHA_2 555 561 PF00498 0.742
LIG_FHA_2 87 93 PF00498 0.714
LIG_Integrin_RGD_1 595 597 PF01839 0.627
LIG_LIR_Apic_2 337 342 PF02991 0.564
LIG_LIR_Apic_2 617 621 PF02991 0.736
LIG_LIR_Gen_1 167 176 PF02991 0.584
LIG_LIR_Gen_1 318 327 PF02991 0.529
LIG_LIR_Gen_1 416 425 PF02991 0.572
LIG_LIR_Gen_1 535 544 PF02991 0.581
LIG_LIR_Gen_1 613 622 PF02991 0.704
LIG_LIR_Gen_1 754 762 PF02991 0.748
LIG_LIR_Gen_1 843 854 PF02991 0.649
LIG_LIR_Nem_3 167 172 PF02991 0.594
LIG_LIR_Nem_3 318 323 PF02991 0.506
LIG_LIR_Nem_3 344 350 PF02991 0.493
LIG_LIR_Nem_3 416 420 PF02991 0.459
LIG_LIR_Nem_3 505 511 PF02991 0.461
LIG_LIR_Nem_3 535 539 PF02991 0.588
LIG_LIR_Nem_3 613 618 PF02991 0.705
LIG_LIR_Nem_3 754 758 PF02991 0.749
LIG_LIR_Nem_3 843 849 PF02991 0.654
LIG_LIR_Nem_3 9 15 PF02991 0.579
LIG_OCRL_FandH_1 469 481 PF00620 0.486
LIG_Pex14_1 2 6 PF04695 0.436
LIG_Pex14_1 346 350 PF04695 0.494
LIG_PTB_Apo_2 746 753 PF02174 0.598
LIG_REV1ctd_RIR_1 468 477 PF16727 0.500
LIG_SH2_CRK 287 291 PF00017 0.566
LIG_SH2_CRK 508 512 PF00017 0.458
LIG_SH2_CRK 653 657 PF00017 0.661
LIG_SH2_NCK_1 122 126 PF00017 0.730
LIG_SH2_NCK_1 287 291 PF00017 0.479
LIG_SH2_NCK_1 653 657 PF00017 0.661
LIG_SH2_SRC 122 125 PF00017 0.646
LIG_SH2_SRC 339 342 PF00017 0.590
LIG_SH2_SRC 425 428 PF00017 0.454
LIG_SH2_SRC 431 434 PF00017 0.492
LIG_SH2_STAP1 425 429 PF00017 0.440
LIG_SH2_STAT5 175 178 PF00017 0.375
LIG_SH2_STAT5 339 342 PF00017 0.590
LIG_SH2_STAT5 401 404 PF00017 0.491
LIG_SH2_STAT5 431 434 PF00017 0.485
LIG_SH3_1 326 332 PF00018 0.519
LIG_SH3_1 519 525 PF00018 0.587
LIG_SH3_1 653 659 PF00018 0.660
LIG_SH3_3 326 332 PF00018 0.519
LIG_SH3_3 483 489 PF00018 0.649
LIG_SH3_3 519 525 PF00018 0.550
LIG_SH3_3 527 533 PF00018 0.587
LIG_SH3_3 547 553 PF00018 0.383
LIG_SH3_3 577 583 PF00018 0.693
LIG_SH3_3 653 659 PF00018 0.660
LIG_SH3_3 692 698 PF00018 0.676
LIG_SUMO_SIM_anti_2 645 650 PF11976 0.625
LIG_SUMO_SIM_anti_2 807 817 PF11976 0.553
LIG_SUMO_SIM_par_1 63 72 PF11976 0.485
LIG_SUMO_SIM_par_1 697 704 PF11976 0.721
LIG_SUMO_SIM_par_1 807 817 PF11976 0.678
LIG_TRAF2_1 535 538 PF00917 0.576
LIG_TRAF2_1 557 560 PF00917 0.815
LIG_TRAF2_1 561 564 PF00917 0.772
LIG_TRAF2_1 569 572 PF00917 0.525
LIG_TRFH_1 653 657 PF08558 0.661
LIG_TYR_ITIM 506 511 PF00017 0.462
LIG_WRC_WIRS_1 467 472 PF05994 0.471
LIG_WRC_WIRS_1 752 757 PF05994 0.613
MOD_CDK_SPxxK_3 784 791 PF00069 0.734
MOD_CK1_1 139 145 PF00069 0.705
MOD_CK1_1 220 226 PF00069 0.662
MOD_CK1_1 244 250 PF00069 0.594
MOD_CK1_1 373 379 PF00069 0.639
MOD_CK1_1 413 419 PF00069 0.581
MOD_CK1_1 456 462 PF00069 0.644
MOD_CK1_1 502 508 PF00069 0.569
MOD_CK1_1 665 671 PF00069 0.682
MOD_CK1_1 714 720 PF00069 0.797
MOD_CK2_1 224 230 PF00069 0.796
MOD_CK2_1 354 360 PF00069 0.656
MOD_CK2_1 507 513 PF00069 0.451
MOD_CK2_1 532 538 PF00069 0.583
MOD_CK2_1 554 560 PF00069 0.740
MOD_CK2_1 566 572 PF00069 0.515
MOD_Cter_Amidation 572 575 PF01082 0.720
MOD_GlcNHglycan 138 141 PF01048 0.787
MOD_GlcNHglycan 142 145 PF01048 0.812
MOD_GlcNHglycan 189 193 PF01048 0.482
MOD_GlcNHglycan 219 222 PF01048 0.662
MOD_GlcNHglycan 226 229 PF01048 0.730
MOD_GlcNHglycan 233 236 PF01048 0.701
MOD_GlcNHglycan 242 246 PF01048 0.385
MOD_GlcNHglycan 251 254 PF01048 0.616
MOD_GlcNHglycan 258 261 PF01048 0.691
MOD_GlcNHglycan 356 359 PF01048 0.703
MOD_GlcNHglycan 388 391 PF01048 0.634
MOD_GlcNHglycan 412 415 PF01048 0.591
MOD_GlcNHglycan 449 452 PF01048 0.636
MOD_GlcNHglycan 639 642 PF01048 0.728
MOD_GlcNHglycan 662 667 PF01048 0.748
MOD_GlcNHglycan 670 674 PF01048 0.689
MOD_GlcNHglycan 780 783 PF01048 0.721
MOD_GlcNHglycan 835 839 PF01048 0.699
MOD_GlcNHglycan 842 845 PF01048 0.594
MOD_GSK3_1 136 143 PF00069 0.745
MOD_GSK3_1 215 222 PF00069 0.579
MOD_GSK3_1 224 231 PF00069 0.667
MOD_GSK3_1 254 261 PF00069 0.756
MOD_GSK3_1 288 295 PF00069 0.393
MOD_GSK3_1 33 40 PF00069 0.503
MOD_GSK3_1 354 361 PF00069 0.714
MOD_GSK3_1 366 373 PF00069 0.636
MOD_GSK3_1 376 383 PF00069 0.699
MOD_GSK3_1 453 460 PF00069 0.656
MOD_GSK3_1 544 551 PF00069 0.600
MOD_GSK3_1 63 70 PF00069 0.525
MOD_GSK3_1 665 672 PF00069 0.661
MOD_GSK3_1 819 826 PF00069 0.765
MOD_GSK3_1 836 843 PF00069 0.497
MOD_GSK3_1 86 93 PF00069 0.762
MOD_N-GLC_1 481 486 PF02516 0.622
MOD_N-GLC_1 637 642 PF02516 0.732
MOD_NEK2_1 152 157 PF00069 0.444
MOD_NEK2_1 188 193 PF00069 0.564
MOD_NEK2_1 246 251 PF00069 0.591
MOD_NEK2_1 292 297 PF00069 0.413
MOD_NEK2_1 378 383 PF00069 0.550
MOD_NEK2_1 42 47 PF00069 0.486
MOD_NEK2_1 432 437 PF00069 0.482
MOD_NEK2_1 453 458 PF00069 0.693
MOD_NEK2_1 48 53 PF00069 0.613
MOD_NEK2_1 598 603 PF00069 0.705
MOD_NEK2_1 67 72 PF00069 0.479
MOD_NEK2_1 711 716 PF00069 0.688
MOD_NEK2_2 466 471 PF00069 0.471
MOD_NEK2_2 514 519 PF00069 0.553
MOD_PIKK_1 220 226 PF00454 0.763
MOD_PIKK_1 228 234 PF00454 0.670
MOD_PIKK_1 246 252 PF00454 0.570
MOD_PIKK_1 563 569 PF00454 0.766
MOD_PKA_1 766 772 PF00069 0.721
MOD_PKA_2 165 171 PF00069 0.613
MOD_PKA_2 354 360 PF00069 0.612
MOD_PKA_2 573 579 PF00069 0.707
MOD_PKA_2 598 604 PF00069 0.720
MOD_PKA_2 766 772 PF00069 0.721
MOD_PKB_1 134 142 PF00069 0.730
MOD_PKB_1 765 773 PF00069 0.608
MOD_Plk_1 188 194 PF00069 0.463
MOD_Plk_1 33 39 PF00069 0.503
MOD_Plk_1 366 372 PF00069 0.688
MOD_Plk_1 68 74 PF00069 0.491
MOD_Plk_2-3 427 433 PF00069 0.448
MOD_Plk_2-3 507 513 PF00069 0.529
MOD_Plk_2-3 86 92 PF00069 0.714
MOD_Plk_4 262 268 PF00069 0.576
MOD_Plk_4 288 294 PF00069 0.487
MOD_Plk_4 342 348 PF00069 0.556
MOD_Plk_4 427 433 PF00069 0.408
MOD_Plk_4 466 472 PF00069 0.474
MOD_Plk_4 507 513 PF00069 0.541
MOD_Plk_4 711 717 PF00069 0.690
MOD_ProDKin_1 107 113 PF00069 0.511
MOD_ProDKin_1 254 260 PF00069 0.684
MOD_ProDKin_1 313 319 PF00069 0.444
MOD_ProDKin_1 325 331 PF00069 0.519
MOD_ProDKin_1 549 555 PF00069 0.540
MOD_ProDKin_1 6 12 PF00069 0.595
MOD_ProDKin_1 784 790 PF00069 0.693
MOD_ProDKin_1 90 96 PF00069 0.800
MOD_SUMO_rev_2 632 637 PF00179 0.740
TRG_DiLeu_BaEn_1 507 512 PF01217 0.461
TRG_DiLeu_LyEn_5 483 488 PF01217 0.650
TRG_ENDOCYTIC_2 287 290 PF00928 0.469
TRG_ENDOCYTIC_2 425 428 PF00928 0.459
TRG_ENDOCYTIC_2 508 511 PF00928 0.461
TRG_ENDOCYTIC_2 658 661 PF00928 0.658
TRG_ER_diArg_1 238 241 PF00400 0.583
TRG_ER_diArg_1 605 608 PF00400 0.725
TRG_ER_diArg_1 706 709 PF00400 0.726
TRG_ER_diArg_1 765 767 PF00400 0.747
TRG_ER_diArg_1 803 805 PF00400 0.700
TRG_NES_CRM1_1 410 421 PF08389 0.448
TRG_NLS_MonoExtC_3 133 138 PF00514 0.759
TRG_NLS_MonoExtN_4 134 139 PF00514 0.761

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6V8 Leptomonas seymouri 46% 95%
A0A3S5H5P2 Leishmania donovani 100% 100%
A4H4J4 Leishmania braziliensis 73% 98%
E9AKQ6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 88% 100%
Q4QJ51 Leishmania major 92% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS