Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_011829868.1 MPE_RS11480 2-hydroxymuconic semialdehyde dehydrogenase
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000015725.1:WP_011829868.1 Length = 484 Score = 317 bits (811), Expect = 8e-91 Identities = 181/483 (37%), Positives = 279/483 (57%), Gaps = 17/483 (3%) Query: 23 FINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPAK 82 FI+GE+ A ++TF PV L + ++D A++AARG +G+W AK Sbjct: 7 FIDGEFVAT--DKTFANRAPVDNRVLGLVHEAGRAEVDAAVAAARGAL-KGEWGRMPVAK 63 Query: 83 RKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGEV 142 R +L +AD + ++ E DTGKP+ + DIP A + +A+ I V E Sbjct: 64 RVELLYAVADEINRRFDDFLAAEIADTGKPLSLASHIDIPRGAANFKVFADIIKNVPAET 123 Query: 143 ATTSSHE----LAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPL 198 ++ + L VR PVGV+ + PWN PLLL WK+GPALA GN+V++KPSE++P Sbjct: 124 FEMATPDGGQALNYAVRTPVGVVGVVCPWNLPLLLMTWKVGPALACGNTVVVKPSEETPA 183 Query: 199 SAIRLAGLAKEAGLPDGVLNVVTGFGHE-AGQALSRHNDIDAIAFTGSTRTGKQLLKDAG 257 +A L + ++ G+P GV NVV GFG + AG L++H D+DAI FTG TRTG+ ++ A Sbjct: 184 TATLLGEVMQKVGMPKGVYNVVHGFGPDSAGAFLTQHPDVDAITFTGETRTGEAIMAAAA 243 Query: 258 DSNMKRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADE 317 ++ V E GGK+A IVFAD D +A + F N GQVC+ R+ ++ I ++ Sbjct: 244 -KGVRPVSFELGGKNAGIVFADA-DFDKAVAGITRSAFENCGQVCLGTERVYVQRPIFEK 301 Query: 318 FLALLKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDG----RNA 373 F+ LK +A+ + G +P +G LI H D V S+ R+ +G ++ G + + Sbjct: 302 FVQALKAKAEALKIGPSEEPGVGLGPLISAEHRDKVLSYYRKAVEQGATVVTGGGVPKMS 361 Query: 374 GLAAA---IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVW 430 G A + PTI+ + +A++ REEIFGP + F +EE+A+ LAN + YGL VW Sbjct: 362 GALAEGHWVQPTIWTGLPESAAVIREEIFGPCCHIAPFDTEEEAIALANATDYGLATTVW 421 Query: 431 TRDLSRAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIW 490 T++L AHR++R+++ G ++N++ D+ FGG K SG GR+ +H+LE +TEL+ + Sbjct: 422 TQNLGTAHRVARQVEVGICWINSWFLRDLRTAFGGAKASGIGREGGVHSLEFYTELRNVC 481 Query: 491 ISL 493 + L Sbjct: 482 VKL 484 Lambda K H 0.317 0.133 0.389 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: 583 Number of extensions: 34 Number of successful extensions: 7 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: 495 Length of database: 484 Length adjustment: 34 Effective length of query: 461 Effective length of database: 450 Effective search space: 207450 Effective search space used: 207450 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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