Alignments for a candidate for BPHYT_RS34245 in Tatumella morbirosei LMG 23360

GapMind for catabolism of small carbon sources

Alignments for a candidate for BPHYT_RS34245 in Tatumella morbirosei LMG 23360

Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_038023703.1 HA49_RS16050 sugar ABC transporter ATP-binding protein

Query= uniprot:B2T9V9
         (510 letters)



>NCBI__GCF_000757425.2:WP_038023703.1
          Length = 506

 Score =  286 bits (732), Expect = 1e-81
 Identities = 167/485 (34%), Positives = 268/485 (55%), Gaps = 2/485 (0%)

Query: 7   ELTSSVPVVEALEVTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKP 66
           EL+    ++    ++KRF    AL+DVS  +  GE  AL+G NGAGKSTL+ +LTG+   
Sbjct: 2   ELSQDTGLLTLKNISKRFPGVKALDDVSFSLRKGEIMALLGENGAGKSTLIKVLTGVYTR 61

Query: 67  DTGEVRFSGAAAPSIADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRGGVIDWQA 126
           D G +  +G      +   A    +  VYQ   ++ ++SVA+NLF+ R+P R G+ID + 
Sbjct: 62  DQGSILLNGREINPRSTAQAQESGIGTVYQEVNLLPNMSVADNLFMGREPRRFGLIDRRT 121

Query: 127 MRRDARALLDHWKIDVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTAQLDGDEI 186
           + R A  LL  +  ++   A  G  SV  +Q++ I RA+    + +ILDEPTA LD  E+
Sbjct: 122 LNRKASELLREYGFELDVTAPLGVFSVAMQQIIAICRAVDLSGQILILDEPTASLDTSEV 181

Query: 187 KRLFRRISELQREGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPREQLIEAM 246
           + LF  + +L+  G++ +F++H L +VY I   +TVLR+ R++ +   + LP+ +LI+ M
Sbjct: 182 EMLFTLMEKLKARGMSLIFVTHFLDQVYRITDRITVLRNGRYVATRDTATLPQLELIKLM 241

Query: 247 TGERGGLAVADAAARGALPADTAVALELKELTGADYEGVSFTVKRGEVVGLTGATSSGRT 306
            G R  L+ +       L ++  V    +     D E     V+ GE+VGL G   SGRT
Sbjct: 242 LG-RELLSTSLQRQGRTLHSENPVVSFSQYGRKGDIEPFDLAVRPGEIVGLAGLLGSGRT 300

Query: 307 SVAEAIAGLRAAKRGTISVDGAILPPGDVPASLAHGIGCVPKDRHHEGLVLTQSVAENAS 366
             AE + G+R A +GT S+ GA         +   GIG  P+DR  +G++   SV EN  
Sbjct: 301 ETAEVLFGIRRADQGTASIRGASQNIRTPARASRAGIGFCPEDRKTDGIIGAASVRENII 360

Query: 367 MTIARVLGKFGIAAPAKKNAFGQKMIDALGIVAQGPEHVVSGLSGGNQQKVVMARALATN 426
           + +    G     +  ++    +++I +LGI     E  V  LSGGNQQKV+++R L T 
Sbjct: 361 LALQAQRGWLRPLSRHQQTEIAERLIKSLGIRTPDVEQPVELLSGGNQQKVLLSRWLVTR 420

Query: 427 PNVLVLIDPTAGVDVKSKEALLSVVDRVREEGKAVLVVSGELDDL-RTCDRVLVMFRGRV 485
           P  L+L +PT G+D+ +   ++ +++ +  +G A+LV+S EL++L    DRV+++   R 
Sbjct: 421 PQFLILDEPTRGIDIGAHAEIIRLIESLCADGLALLVISSELEELVGYADRVIILRDHRQ 480

Query: 486 AAEFP 490
            AE P
Sbjct: 481 VAEIP 485



 Score = 73.9 bits (180), Expect = 1e-17
 Identities = 71/252 (28%), Positives = 106/252 (42%), Gaps = 14/252 (5%)

Query: 8   LTSSVPVVEALEVTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKPD 67
           L S  PVV       ++G    +    + V PGE   L G  G+G++    +L G+R+ D
Sbjct: 258 LHSENPVVSF----SQYGRKGDIEPFDLAVRPGEIVGLAGLLGSGRTETAEVLFGIRRAD 313

Query: 68  TGEVRFSGAAAPSIADRDAWRERVA-CVYQHST--IIRDLSVAENLFINRQPLRGGV--I 122
            G     GA+        A R  +  C     T  II   SV EN+ +  Q  RG +  +
Sbjct: 314 QGTASIRGASQNIRTPARASRAGIGFCPEDRKTDGIIGAASVRENIILALQAQRGWLRPL 373

Query: 123 DWQAMRRDARALLDHWKI---DVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTA 179
                   A  L+    I   DV +      LS   +Q V ++R L    +F+ILDEPT 
Sbjct: 374 SRHQQTEIAERLIKSLGIRTPDVEQPVEL--LSGGNQQKVLLSRWLVTRPQFLILDEPTR 431

Query: 180 QLDGDEIKRLFRRISELQREGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPR 239
            +D      + R I  L  +G+  L IS  L+E+      V +LRD R +   P+  L  
Sbjct: 432 GIDIGAHAEIIRLIESLCADGLALLVISSELEELVGYADRVIILRDHRQVAEIPLERLSV 491

Query: 240 EQLIEAMTGERG 251
             ++ A+    G
Sbjct: 492 GTIMTAIADGGG 503


Lambda     K      H
   0.318    0.134    0.377 

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: 549
Number of extensions: 37
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 510
Length of database: 506
Length adjustment: 34
Effective length of query: 476
Effective length of database: 472
Effective search space:   224672
Effective search space used:   224672
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.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources