GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Maridesulfovibrio bastinii DSM 16055

Align Histidinol-phosphate aminotransferase 1; EC 2.6.1.9; Imidazole acetol-phosphate transaminase 1 (uncharacterized)
to candidate WP_027177759.1 G496_RS0101750 cobyric acid synthase

Query= curated2:Q3AD52
         (349 letters)



>NCBI__GCF_000429985.1:WP_027177759.1
          Length = 880

 Score =  125 bits (315), Expect = 3e-33
 Identities = 98/327 (29%), Positives = 158/327 (48%), Gaps = 16/327 (4%)

Query: 30  ANENPYLFPKSLLEEIFSKIGTRDFPLYPDPLAGRLRIRLSEKLGVLPENIVLGNGSDEL 89
           AN NP   P  L +EI   I   +   YPDP    L +   EK  V P   + GNG+ EL
Sbjct: 40  ANINPIGPPSWLRQEILHSID--EIECYPDPECSELTLAACEKFSVWPNECIAGNGASEL 97

Query: 90  ILCLYLAFGGYGRIALSFSPSFVMYRHHAFVT--QTEFFEVSYRDDFSLDLDETKKAIEK 147
            LC+    GG+ +  +   P +V Y     +   + E  ++   + F  D +     +EK
Sbjct: 98  -LCIAARLGGFKKAVIPV-PCYVDYERACTLAGLKIEKIQLGMENGFQPDFEAIAAILEK 155

Query: 148 YQPHLVFLANPNNPTGTLVDIETIKKLL--AYDHLLVVDEAYVEFSGVSAIDLLKKYQNL 205
             P LVFLA PNNPTGT  D   +++L     +   ++DE++  F       + K+ +N+
Sbjct: 156 -SPALVFLAQPNNPTGTTFDTGKLRELANRYSESRFIIDESFAAFVEDLDRTVKKRPKNV 214

Query: 206 VILRTFSKARALAGLRLGYLVASVDVVKEIIKVKNPYNVNVFSQIAGEVVLANEEVFQGE 265
           + + + +K  A+ GLRLG   +S ++++++ ++   ++VN+ +Q  G   L + +  +  
Sbjct: 215 ITIVSLTKFYAIPGLRLGLAFSSPEIIQKMREIMPCWSVNLMAQRVGTRCLKDSDYSELT 274

Query: 266 IKEIVAERERLYNQLASL-GLKPVKSHANFILVE---FGEKAKKIHQELINHGILVRY-- 319
            KE    R  L   L+ + GL+     ANF+L +    G  A  I   LI++ I VR   
Sbjct: 275 QKETTRLRNELVAGLSEIPGLRVFPGEANFLLCQVQRVGMNASAIINHLISNKIAVRQCD 334

Query: 320 -LGGALANYLRITVGTPEENRQLLKKL 345
              G   +Y RI V T  ENR L+ +L
Sbjct: 335 NFDGLDDSYFRIAVRTDAENRLLVDEL 361


Lambda     K      H
   0.321    0.141    0.398 

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: 618
Number of extensions: 32
Number of successful extensions: 3
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: 349
Length of database: 880
Length adjustment: 36
Effective length of query: 313
Effective length of database: 844
Effective search space:   264172
Effective search space used:   264172
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 (21.8 bits)
S2: 53 (25.0 bits)

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

Links

Downloads

Related tools

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