GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Rhodobacter sphaeroides ATCC 17029

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_002721052.1 RSPH17029_RS12705 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000015985.1:WP_002721052.1
          Length = 369

 Score =  180 bits (457), Expect = 4e-50
 Identities = 136/363 (37%), Positives = 191/363 (52%), Gaps = 39/363 (10%)

Query: 5   ICLIEGDGIGHEVIPAARRVL----EATGLPLEFVEAEAGWETFERRGTSVPEETVEKIL 60
           + ++ GDGIG EV+   +R++    E  G+  +  E   G   ++  GT + +ET+ +  
Sbjct: 6   LLILAGDGIGPEVMAEVKRIIGWFGEKRGVTFDVSEDLVGGAAYDAHGTPLADETMARAQ 65

Query: 61  SCHATLFGAATSPTRKVPGFF-----GAIRYLRRRLDLYANVRPAK--------SRPVPG 107
              A L GA   P   V  F      G +R LR+ +DLYAN+RPA+        S     
Sbjct: 66  EVDAVLLGAVGGPKYDVLDFSVKPERGLLR-LRKEMDLYANLRPAQCFDALADFSSLKRD 124

Query: 108 SRPGVDLVIVRENTEGLYVEQERRYLD------VAIADAVISKKASERIGRAALRIAEGR 161
              G+D++IVRE T G+Y  + R            +     + +   R+ R+A  +A  R
Sbjct: 125 IVAGLDIMIVRELTSGVYFGEPRGIFPDNEGGRFGVNTQRYTTEEIRRVARSAFELARRR 184

Query: 162 PRKTLHIAHKANVLPLTQGLFLDTVKEVA-KDFPLVNVQDIIVDNCAMQLVMRPERFDVI 220
             +   +  KANV+  +  L+ + V+ V   ++P V +  +  DN AMQLV  P +FDVI
Sbjct: 185 NNRVCSM-EKANVME-SGILWREEVQWVHDNEYPDVELSHMYADNGAMQLVRWPRQFDVI 242

Query: 221 VTTNLLGDILSDLAAGLVGGLGLAPSGNI------GDTTAVFEPVHGSAPDIAGKGIANP 274
           VT NL GDILSD AA L G LG+ PS ++      G   A++EPVHGSAPDIAG+G ANP
Sbjct: 243 VTDNLFGDILSDCAAMLTGSLGMLPSASLGAPMANGRPKALYEPVHGSAPDIAGQGKANP 302

Query: 275 TAAILSAAMMLDYLGEK-EAAKRVEKAVDLVLERGPRTPDL-----GGDATTEAFTEAVV 328
            A ILS AM L Y  +  E A R+EKAV+ VL  G RT DL     G   +T    +AV+
Sbjct: 303 IACILSFAMALRYSFDMGEEATRLEKAVETVLADGVRTADLMGPEGGTPVSTSGMGDAVL 362

Query: 329 EAL 331
            AL
Sbjct: 363 AAL 365


Lambda     K      H
   0.319    0.137    0.391 

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: 326
Number of extensions: 20
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: 334
Length of database: 369
Length adjustment: 29
Effective length of query: 305
Effective length of database: 340
Effective search space:   103700
Effective search space used:   103700
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 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