Align D-mannose isomerase (EC 5.3.1.7) (characterized)
to candidate AO356_05200 AO356_05200 sugar isomerase
Query= reanno::WCS417:GFF4325 (419 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_05200 Length = 419 Score = 640 bits (1651), Expect = 0.0 Identities = 300/402 (74%), Positives = 335/402 (83%) Query: 9 SSWLNAPAHYVWLAAEGQRLLAFAKASRLPDGFGNLDDKGQLPADAHAETMNTARMTHSF 68 SSWLNAPAH WLAAEG RLLAFAKAS+LPDGFGNLD+ G+LPADA AETMNTARMTHSF Sbjct: 9 SSWLNAPAHQQWLAAEGLRLLAFAKASKLPDGFGNLDELGRLPADARAETMNTARMTHSF 68 Query: 69 AMAHALGLPGYAELVAHGVAALSGALRDSEHGGWFAAPHALDGNRGKAAYLHAFVALAAS 128 AMAH GLPG+AELV HG+ AL+G LRD+EHGGWFA + GKAAYLHAFVALAAS Sbjct: 69 AMAHIQGLPGFAELVDHGIQALNGRLRDAEHGGWFATTRPDEDGAGKAAYLHAFVALAAS 128 Query: 129 SAVVAGAPGASTLLNDAIHIIDHFFWSEEEGVMLESFAQDWSGVEAYRGANSNMHATEAF 188 SAVVA PGA+ LL++A+ IID FW EEEG + ESF +DWS EAYRGANSNMHATEAF Sbjct: 129 SAVVAQRPGAAALLDEAVRIIDEHFWCEEEGALRESFNRDWSEEEAYRGANSNMHATEAF 188 Query: 189 LALADVTGDTRWLDRALRIVERVIHTHAAGNQFMVIEHFDTHWHPLLGYNEDNPADGFRP 248 LALAD T D RWL RALRIVERVIH HAA N ++V+EHFD HW PL YN+DNPADGFRP Sbjct: 189 LALADATDDPRWLVRALRIVERVIHGHAAANDYLVVEHFDRHWQPLHEYNQDNPADGFRP 248 Query: 249 YGITPGHGFEWARLVLHLEAARLQAGLVTPEWLVADAKRLFASACEYAWSVDGAPGIVYT 308 YG TPGHGFEWARL+LHLEAAR+Q G++TP WL DA++LF C + W VDGAPGIVYT Sbjct: 249 YGTTPGHGFEWARLLLHLEAARVQIGMLTPGWLAQDAQKLFDQNCRHGWDVDGAPGIVYT 308 Query: 309 LDWNHRPVVRERLHWTHAEASAAAQALLKRTGELHYETWYRRFWEFCETHFIDRLHGSWH 368 LDW++R VVR RLHW HAEA+AAA ALLKRT E YE WYR FWEFC+ HFIDR +GSWH Sbjct: 309 LDWDNRAVVRHRLHWVHAEAAAAASALLKRTDEAKYEAWYRCFWEFCDKHFIDRCNGSWH 368 Query: 369 HELSPHNQPSSNIWGGKPDLYHAWQAVLLPALPLAPSMASAI 410 HEL P N+PS++IW GKPDLYHAWQAVL+P LPLAPSMASA+ Sbjct: 369 HELDPQNRPSADIWPGKPDLYHAWQAVLIPRLPLAPSMASAL 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: 782 Number of extensions: 29 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:
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