Align D-mannose isomerase (EC 5.3.1.7) (characterized)
to candidate PfGW456L13_1893 N-acylglucosamine 2-epimerase (EC 5.1.3.8)
Query= reanno::WCS417:GFF4325 (419 letters) >lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1893 N-acylglucosamine 2-epimerase (EC 5.1.3.8) Length = 419 Score = 635 bits (1637), Expect = 0.0 Identities = 300/402 (74%), Positives = 335/402 (83%) Query: 9 SSWLNAPAHYVWLAAEGQRLLAFAKASRLPDGFGNLDDKGQLPADAHAETMNTARMTHSF 68 SSWLNAPAH WLA EG RLL FAKAS+LP+GFGNLD+KG+LP+DA A+TMNTARMTHSF Sbjct: 9 SSWLNAPAHQQWLATEGLRLLTFAKASKLPEGFGNLDEKGRLPSDAQAQTMNTARMTHSF 68 Query: 69 AMAHALGLPGYAELVAHGVAALSGALRDSEHGGWFAAPHALDGNRGKAAYLHAFVALAAS 128 AMAH GLPG+AELV HGVAAL G LRD+ +GGWFA DGN GK AYLHAFVALAAS Sbjct: 69 AMAHIQGLPGFAELVDHGVAALRGPLRDTLYGGWFATAEHRDGNTGKNAYLHAFVALAAS 128 Query: 129 SAVVAGAPGASTLLNDAIHIIDHFFWSEEEGVMLESFAQDWSGVEAYRGANSNMHATEAF 188 SAVVA PGA LL+DAI IID +FWSEEEG M ESF +DWS EAYRGANSNMHATEAF Sbjct: 129 SAVVAQRPGAQALLDDAIDIIDTYFWSEEEGAMRESFNRDWSEEEAYRGANSNMHATEAF 188 Query: 189 LALADVTGDTRWLDRALRIVERVIHTHAAGNQFMVIEHFDTHWHPLLGYNEDNPADGFRP 248 LALADVT D RWL RA RIVERVIH HAA N ++VIEHFD W PL YN DNPADGFRP Sbjct: 189 LALADVTDDNRWLSRAHRIVERVIHGHAAANDYLVIEHFDRAWQPLRDYNRDNPADGFRP 248 Query: 249 YGITPGHGFEWARLVLHLEAARLQAGLVTPEWLVADAKRLFASACEYAWSVDGAPGIVYT 308 YG TPGHGFEWARL+LHLEA+R++AG++TP WLV DA++LF C + W VDGAPGIVYT Sbjct: 249 YGTTPGHGFEWARLLLHLEASRVKAGMLTPGWLVTDAQKLFEHNCFHGWDVDGAPGIVYT 308 Query: 309 LDWNHRPVVRERLHWTHAEASAAAQALLKRTGELHYETWYRRFWEFCETHFIDRLHGSWH 368 LDW+++ VVR RLHWTH EASAAA ALLKRTG+ YE WYR FWEFC++HFIDR GSWH Sbjct: 309 LDWDNKAVVRHRLHWTHCEASAAASALLKRTGDEQYEHWYRLFWEFCDSHFIDREDGSWH 368 Query: 369 HELSPHNQPSSNIWGGKPDLYHAWQAVLLPALPLAPSMASAI 410 HEL P N+PS++IW GKPDLYHAWQAVL+P L LAPSMA+A+ Sbjct: 369 HELDPQNRPSADIWPGKPDLYHAWQAVLIPRLALAPSMATAL 410 Lambda K H 0.321 0.134 0.442 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 803 Number of extensions: 34 Number of successful extensions: 1 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 419 Length of database: 419 Length adjustment: 32 Effective length of query: 387 Effective length of database: 387 Effective search space: 149769 Effective search space used: 149769 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory