GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatA in Azospirillum brasilense Sp245

Align Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate AZOBR_RS06950 AZOBR_RS06950 ABC transporter

Query= TCDB::B8H229
         (515 letters)



>FitnessBrowser__azobra:AZOBR_RS06950
          Length = 520

 Score =  275 bits (704), Expect = 2e-78
 Identities = 179/481 (37%), Positives = 264/481 (54%), Gaps = 16/481 (3%)

Query: 4   LDVSQVSKSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFA 63
           L++  ++K FPG  A DQVDLV+  GE+HALLGENGAGKSTL+KI+     ADAG + + 
Sbjct: 13  LELRGITKRFPGCLANDQVDLVLRPGEIHALLGENGAGKSTLVKIIYGVLHADAGRIQWN 72

Query: 64  GQVLDPRDAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRRLGLVDWSRLRADAQA 123
           G      D P   ++LGI  ++Q F+LF  L+VAEN+ LG +  + G +D   L A    
Sbjct: 73  GHDTHIPD-PAGARRLGIGMVFQHFSLFDTLTVAENISLGLD--QPGPID--ALSARIAE 127

Query: 124 LLNDLGLPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHAII 183
           +    GL L+P   V  L+V E+Q VEI + +  + +L+IMDEPT+ L+ +E  RL   +
Sbjct: 128 VSERYGLSLDPRRHVHNLSVGERQRVEIVRCLLQDPKLLIMDEPTSVLTPQEATRLFETL 187

Query: 184 AGLKARSVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVADMVRLMVGRHVEF 243
             L A   +++Y+SH+L E++A+CD  TV+R GR V S D        +  +M+G  +  
Sbjct: 188 RRLAAEGCTILYISHKLEEIRALCDTATVLRGGRVVGSCDPRRETARSLAEMMIGTELST 247

Query: 244 ERRKRRRPPGAVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLAR 303
             R  +   GA  L+V  ++  +    A   L+ VSF  R GEI+G+AG+ G G+ +L  
Sbjct: 248 PERLPQGEAGAAKLQVRHLSTTSDNPFATN-LKDVSFEVRAGEILGIAGVAGNGQAELMA 306

Query: 304 LIFG----ADPIAAGRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSIRRN-- 357
            + G     DP +   V ++ +P     PR+    G+  VPE+R  +G   + S+  N  
Sbjct: 307 ALSGEALVPDPAS---VAIEGRPAGHLGPRERRLLGLAFVPEERLGRGAVPELSLSENAL 363

Query: 358 LSLPSLKALSALGQWVDERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAM 417
           LS  + + L   G     RA R   E       +           LSGGN QK ++GR +
Sbjct: 364 LSGYAREPLVRSGLVHFGRA-RSYAERIIGAFNVVTHGHRAEARSLSGGNLQKFIIGREI 422

Query: 418 ALTPKVLIVDEPTRGIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFRE 477
              P++L+V +PT G+D GA A +H+ L DLA  G AV+VIS +L E+  +SDRI V   
Sbjct: 423 LQKPRLLVVGQPTWGVDAGAAAAIHRALIDLARAGAAVLVISQDLDELFVLSDRIAVLFH 482

Query: 478 G 478
           G
Sbjct: 483 G 483



 Score = 80.5 bits (197), Expect = 1e-19
 Identities = 75/252 (29%), Positives = 111/252 (44%), Gaps = 25/252 (9%)

Query: 257 LKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLARLIFGADPIAAGRV 316
           L++ G+T   P   A     QV    R GEI  L G  GAG++ L ++I+G     AGR+
Sbjct: 13  LELRGITKRFPGCLAND---QVDLVLRPGEIHALLGENGAGKSTLVKIIYGVLHADAGRI 69

Query: 317 LVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSIRRNLSLP-----SLKALSALGQ 371
             +     +  P  A + GI +V +       F   ++  N+SL       + ALSA   
Sbjct: 70  QWNGHDTHIPDPAGARRLGIGMVFQ---HFSLFDTLTVAENISLGLDQPGPIDALSARIA 126

Query: 372 WVDERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAMALTPKVLIVDEPTR 431
            V ER    L             D    +  LS G +Q+V + R +   PK+LI+DEPT 
Sbjct: 127 EVSERYGLSL-------------DPRRHVHNLSVGERQRVEIVRCLLQDPKLLIMDEPTS 173

Query: 432 GIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFREGVIVADLDAQTATE 491
            +       + + L  LA  G  ++ IS +L E+ A+ D   V R G +V   D +  T 
Sbjct: 174 VLTPQEATRLFETLRRLAAEGCTILYISHKLEEIRALCDTATVLRGGRVVGSCDPRRETA 233

Query: 492 EGLMAYMATGTD 503
             L A M  GT+
Sbjct: 234 RSL-AEMMIGTE 244



 Score = 67.0 bits (162), Expect = 2e-15
 Identities = 65/237 (27%), Positives = 104/237 (43%), Gaps = 16/237 (6%)

Query: 14  PGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSA-AHAADAGTVTFAGQV---LDP 69
           P    L  V   V  GE+  + G  G G++ L+  LS  A   D  +V   G+    L P
Sbjct: 273 PFATNLKDVSFEVRAGEILGIAGVAGNGQAELMAALSGEALVPDPASVAIEGRPAGHLGP 332

Query: 70  RDAPLRRQQLGIATIYQEF---NLFPELSVAENMYLG---REPR-RLGLVDWSRLRADAQ 122
           R+    R+ LG+A + +E       PELS++EN  L    REP  R GLV + R R+ A+
Sbjct: 333 RE----RRLLGLAFVPEERLGRGAVPELSLSENALLSGYAREPLVRSGLVHFGRARSYAE 388

Query: 123 ALLNDLGLPLNPD-APVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHA 181
            ++    +  +   A  R L+    Q   I + +    RL+++ +PT  +       +H 
Sbjct: 389 RIIGAFNVVTHGHRAEARSLSGGNLQKFIIGREILQKPRLLVVGQPTWGVDAGAAAAIHR 448

Query: 182 IIAGLKARSVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVADMVRLMVG 238
            +  L     +V+ +S  L E+  + DR  V+  G    S       V ++  LM G
Sbjct: 449 ALIDLARAGAAVLVISQDLDELFVLSDRIAVLFHGHLSESRPTHHTSVEEIGLLMGG 505


Lambda     K      H
   0.320    0.136    0.380 

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: 640
Number of extensions: 31
Number of successful extensions: 9
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 3
Length of query: 515
Length of database: 520
Length adjustment: 35
Effective length of query: 480
Effective length of database: 485
Effective search space:   232800
Effective search space used:   232800
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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