GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysT in Hydrogenovibrio halophilus DSM 15072

Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate WP_019895993.1 A377_RS0108985 3-isopropylmalate dehydratase large subunit

Query= curated2:Q8PZT3
         (391 letters)



>NCBI__GCF_000384235.1:WP_019895993.1
          Length = 480

 Score =  220 bits (561), Expect = 6e-62
 Identities = 139/360 (38%), Positives = 186/360 (51%), Gaps = 45/360 (12%)

Query: 75  EGICHQVLPENGFALPGKLLVGADSHSCTYGAFGAFATGVGATDMAEIFATGKLWFKVPE 134
           +GI H V PE G  LPG  LV  DSH+ T+GA GA A GVG +++  + AT  L  K  +
Sbjct: 113 QGIVHVVGPEEGITLPGMTLVCGDSHTATHGALGALAHGVGTSEVEHVLATQCLIQKKMK 172

Query: 135 SFRMTVEGSLDKHVYAKDLTLYLIGKTGIAGATYKAVEFYGQAISELSVAGRMTLCNMAI 194
           +  + V+G L   V  KD+ L +IG+ G AG    A+EF GQ   +++V GRMT+CNMAI
Sbjct: 173 NMLVKVDGQLAPGVTPKDVILAVIGQIGTAGGNGYAIEFGGQVFRDMTVEGRMTVCNMAI 232

Query: 195 EMGAKTGIVPPDEKTFDFLKNRAVAP-----------YEPVYSDPDASYLKEFVYDAGDI 243
           E GA+ G+V  D+KT +++K R  AP           ++ + SD  A + K    D   I
Sbjct: 233 EAGARVGLVAVDDKTIEYVKGRPYAPKGELWEQAVESWQSLVSDEGAVFDKVVEIDGSAI 292

Query: 244 EPQVAC-----------------PHQVDNVKP---------VGEVEGTH-----VDQVFI 272
           EPQV+                    Q D+VK          +G   GT      VD +FI
Sbjct: 293 EPQVSWGTSPEMVGPINGCVPDPDKQADSVKAESIRHALQYMGLTPGTPFVDIGVDYIFI 352

Query: 273 GTCTNGRLEDLEVAASVLKGKKVTVRT---IIIPASRSTLLAAIKNGTMEILLKAGVTLA 329
           G+CTN R+EDL  AA V+KG+KV       +++P S      A   G   I L AG    
Sbjct: 353 GSCTNSRIEDLRAAAEVVKGRKVADSVELAMVVPGSGLVKQQAEAEGLDRIFLDAGFEWR 412

Query: 330 TPGCGPCLGAHQGVLGEGEVCVSTANRNFKGRMGKDGFIYLASPATAAASALTGEITDPR 389
            PGC  CL  +   L  G+ C ST+NRNF+GR G  G  +L SP  AAA+A+ G   D R
Sbjct: 413 NPGCSMCLAMNADKLPAGKHCASTSNRNFEGRQGAGGRTHLVSPEMAAAAAVAGRFVDVR 472


Lambda     K      H
   0.318    0.135    0.401 

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: 480
Number of extensions: 20
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 391
Length of database: 480
Length adjustment: 32
Effective length of query: 359
Effective length of database: 448
Effective search space:   160832
Effective search space used:   160832
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: 51 (24.3 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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